1.  Chen CP, Chern SR, Wu PS, Chen SW, Wu FT, Lee CC, Pan CW, Chen YY, Wang W. 2022. High-level mosaicism for 45,X in 45,X/46, XY at amniocentesis in a pregnancy with a favorable fetal outcome and cytogenetic discrepancy in various tissues. Taiwan J Obstet Gynecol. 61(4):695-699.

2. Chen CP, Hsu TY, Tsai CC, Chern SR, Chen SW, Wu FT, Wu PS, Lee CC, Chen LF, Pan CW, Wang W. 2022. Mosaic trisomy 18 at amniocentesis associated with a favorable fetal outcome in a pregnancy. Taiwan J Obstet Gynecol. 61(4):690-694.

3.  Chen CP, Su JW, Chern SR, Wu PS, Chen SW, Wu FT, Chen WL, Lee MS, Pan CW, Chen YY, Wang W. 2022. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 18 at amniocentesis in a pregnancy with a favorable fetal outcome and maternal uniparental disomy 18. Taiwan J Obstet Gynecol. 61(4):684-689.

4.  Chen CP, Ko TM, Chen TC, Chern SR, Wu PS, Chen SW, Wu FT, Chen WL, Chen YY, Wang W. 2022. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 61(4):677-683.

5.  Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Pan CW, Wang W. 2022. Prenatal diagnosis of pseudomosaicism for trisomy 20 at amniocentesis with a negative non-invasive prenatal testing (NIPT) result in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 61(4):675-676.

6.  Chen CP, Chen SW, Wu PS, Wu FT, Wang W. 2022. A false-positive result at non-invasive prenatal testing due to maternal 17p12 microduplication. Taiwan J Obstet Gynecol. 61(3):532-534.

7.  Chen CP, Su JW, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Chen WL, Lee MS, Pan CW, Wang W. 2022. Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic 46,XX,dup(9)(q22.3q34.1)/ 46,XX at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 61(2):368-371.

8.  Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Lee CC, Chen LF, Wang W. 2022. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 21 associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening. Taiwan J Obstet Gynecol. 61(2):359-363.

9.  Chen CP, Liou JD, Chern SR, Wu PS, Chen SW, Wu FT, Lee MS, Chen YY, Wang W. 2022. Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome. Taiwan J Obstet Gynecol. 61(1):146-149.

10. Chen CP, Lin YH, Wu PS, Chern SR, Chen SW, Wu FT, Lee CC, Pan CW, Chen YY, Wang W. 2022. Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 61(1):138-140.

11. Lee CL, Chuang CK, Tu RY, Chiu HC, Lo YT, Chang YH, Chen YJ, Chou CL, Wu PS, Chen CP, Lin HY, Lin SP. 2021. Increased Diagnostic Yield of Array Comparative Genomic Hybridization for Autism Spectrum Disorder in One Institution in Taiwan. Medicina (Kaunas). 58(1):15.

12. Chen CP, Chern SR, Wu PS, Chen SW, Wu FT, Chen WL, Wang W. 2021. Application of array comparative genomic hybridization analysis for rapid differential diagnosis of a chromosome euchromatic variant of dup 22q13.3 at amniocentesis. Taiwan J Obstet Gynecol. 60(6):1134-1135.

13.  Chen CP, Lan FH, Chern SR, Wu PS, Chen SW, Wu FT, Lee CC, Lee MS, Pan CW, Chen YY, Wang W. 2021. Prenatal diagnosis of mosaic trisomy 16 by amniocentesis in a pregnancy associated with abnormal first-trimester screening result (low PAPP-A and low PlGF), intrauterine growth restriction and a favorable outcome. Taiwan J Obstet Gynecol. 60(6):1107-1111.

14.  Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Lee CC, Pan CW, Wang W. 2021. Prenatal diagnosis of a familial 9p12 amplification inherited from a father carrier. Taiwan J Obstet Gynecol. 60(5):905-906.

15.   Chen CP, Wang PT, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Lee CC, Town DD, Wang W. 2021. Prenatal diagnosis of a familial Y long-arm and chromosome 15 short-arm translocation inherited from a mother carrier. Taiwan J Obstet Gynecol. 60(4):781-783.

16. Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Lee MS, Wang W. 2021. Mosaic Xq duplication, or 46,X,der(X)dup(X)(q22.1q22.2) dup(X)(q25 q22.3)/46,XX at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 60(4):778-780.

17.  Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W. 2021. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result. Taiwan J Obstet Gynecol. 60(4):775-777.

18.  Chen CP, Tsai HT, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Town DD, Chen WL, Lee MS, Wang W. 2021. Prenatal diagnosis of mosaicism for double aneuploidy of 47,XXY and trisomy 7 (48,XXY,+7) at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 60(3):543-548.

19.   Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Town DD, Chen LF, Wang W. 2021. Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus. Taiwan J Obstet Gynecol. 60(3):534-539.

20.  Chen CP, Chen M, Wang LK, Chern SR, Wu PS, Ma GC, Chang SP, Chen SW, Wu FT, Lee CC, Chen YY, Wang W. 2021. Low-level mosaicism for trisomy 16 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome. Taiwan J Obstet Gynecol. 60(2):345-349.

21.   Chen CP, Chern SR, Wu PS, Chen SW, Wu FT, Wang W. 2021. Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects. Taiwan J Obstet Gynecol. 60(2):341-344.

22.   Chen CP, Lin MH, Chen YY, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Lee MS, Pan CW, Wang W. 2021. Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome. Taiwan J Obstet Gynecol. 60(2):335-340.

23.   Chen CP, Lo LM, Ko TM, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Chen LF, Chen YY, Wang W. 2021. Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes. Taiwan J Obstet Gynecol. 60(2):331-334.

24.   Chen CP, Lin SP, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Wang W. 2021. Tetrasomy of 11q13.4-q14.3 due to an intrachromosomal triplication associated with paternal uniparental isodisomy for 11q14.3-qter, intrauterine growth restriction, developmental delay, corpus callosum dysgenesis, microcephaly, congenital heart defects and facial dysmorphism. Taiwan J Obstet Gynecol. 60(1):169-172.

25.  Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Wang W. 2021. Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother. Taiwan J Obstet Gynecol. 60(1):165-168.

26.  Chen CP, Chern SR, Wu PS, Chen SW, Wu FT, Wang W. 2021. Prenatal diagnosis of familial 2p15 microduplication associated with pulmonary artery stenosis, single umbilical artery and left foot postaxial polydactyly on fetal ultrasound. Taiwan J Obstet Gynecol. 60(1):161-164.

27. Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Town DD, Wang W. 2021. Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion. Taiwan J Obstet Gynecol. 60(1):157-160.

28.  Chen CP, Chan CH, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Lee MS, Wang W. 2021. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome. Taiwan J Obstet Gynecol. 60(1):152-156.

29.   Chen CP, Lin CJ, Chen SW, Wu FT, Chern SR, Wu PS, Chen YY, Chen WL, Wang W. 2020. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia. Taiwan J Obstet Gynecol. 59(6):941-944.

30.   Chen CP, Chern SR, Wang LK, Wu PS, Wu FT, Chen YY, Town DD, Pan CW, Wang W. 2020. Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy. Taiwan J Obstet Gynecol. 59(6):938-940.

31.   Chen CP, Ko TM, Huang JP, Chern SR, Wu PS, Chen SW, Wu FT, Chen WL, Lee MS, Wang W. 2020. Prenatal diagnosis of a familial normal euchromatic variant of dup(15)(q11.2q11.2) in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 59(5):770-772.

32.   Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Chen WL, Chen LF, Wang W. 2020. Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin. Taiwan J Obstet Gynecol. 59(5):766-769.

33.   Chen CP, Hsu CY, Chern SR, Wu PS, Chen SW, Wu FT, Wang W. 2020. Prenatal diagnosis of a 1.651-Mb 19q13.42-q13.43 microdeletion in a fetus with micrognathia and bilateral pyelectasis on prenatal ultrasound. Taiwan J Obstet Gynecol. 59(5):763-765.

34.  Chen CP, Liou JD, Seow KM, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Chen LF, Wang W. 2020. Prenatal diagnosis of partial monosomy 2q (2q37.3→ qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results. Taiwan J Obstet Gynecol. 59(5):758-762.

35.  Chen CP, Ko TM, Chen YY, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Chen WL, Pan CW, Wang W. 2020. Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome. Taiwan J Obstet Gynecol. 59(5):754-757.

36.  Chen CP, Hsu TY, Ko TM, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Lee CC, Pan CW, Wang W. 2020. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis. Taiwan J Obstet Gynecol. 59(5):728-735.

37.  Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Chen WL, Wang W. 2020. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound. Taiwan J Obstet Gynecol. 59(4):598-603.

38.  Chen CP, Lin HY, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Fran S, Chen YY, Town DD, Pan CW, Wang W. 2020. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15). Taiwan J Obstet Gynecol. 59(4):580-585.

39.  Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Wang W. 2020. Perinatal cytogenetic discrepancy in a fetus with low-level mosaicism for trisomy 21 and a favorable outcome. Taiwan J Obstet Gynecol. 59(3):440-442.

40.   Chen CP, Wu CY, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Chen WL, Wang W. 2020. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interchromosomal insertion of ins(1;8)(p22.1;q22q23). Taiwan J Obstet Gynecol. 59(3):437-439.

41. Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Pan CW, Wang W. 2020. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion. Taiwan J Obstet Gynecol. 59(3):432-436.

42. Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Chen YY, Wang W. 2020. Wolf-Hirschhorn syndrome: Prenatal diagnosis and molecular cytogenetic characterization of a de novo distal deletion of 4p (4p16.1 → pter) in a fetus with facial cleft and preaxial polydactyly. Taiwan J Obstet Gynecol. 59(3):425-431.

43.  Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen WL, Wang W. 2020. Prenatal diagnosis of mosaicism for a distal 5p deletion in a single colony at amniocentesis in a pregnancy with a favorable outcome and a review of mosaic distal 5p deletion. Taiwan J Obstet Gynecol. 59(2):334-337.

44.   Chen CP, Weng SL, Chern SR, Wu PS, Chen SW, Wu FT, Lee MS, Wang W. 2020. Prenatal diagnosis of mosaicism for trisomy 11 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 59(2):331-333.

45.    Chen CP, Kuo YL, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W. 2020. Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 59(2):327-330.

46.  Chen CP, Chern SR, Wu PS, Chen SW, Lai ST, Wu FT, Town DD, Wang W. 2020. Monozygotic twins discordant for low-level mosaic trisomy 17 at amniocentesis in a pregnancy with a favorable outcome and a literature review of heterokaryotypic monozygotic twins at amniocentesis. Taiwan J Obstet Gynecol. 59(2):306-313.

47.  Chen CP, Chern SR, Wu PS, Chen SW, Lai ST, Wu FT, Town DD, Wang W. 2020. Monozygotic twins discordant for low-level mosaic trisomy 17 at amniocentesis in a pregnancy with a favorable outcome and a literature review of heterokaryotypic monozygotic twins at amniocentesis. Taiwan J Obstet Gynecol. 59(2):306-313.

48.  Chen CP, Lin SY, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Wang W. 2020. Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 59(2):301-305.

49.   Chen CP, Lin YH, Chern SR, Wu PS, Chen SW, Wu FT, Lee MS, Chen YY, Wang W. 2020. Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis. Taiwan J Obstet Gynecol. 59(1):146-149.

50.  Chen CP, Huang JP, Chern SR, Wu PS, Chen SW, Wu FT, Chen WL, Lee MS, Wang W. 2020. Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication. Taiwan J Obstet Gynecol. 59(1):140-145.

51.   Chen CP, Huang JP, Chen SW, Chern SR, Wu PS, Wu FT, Chen WL, Chen LF, Wang W. 2020. Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects. Taiwan J Obstet Gynecol. 59(1):135-139.

52.  Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lee CC, Chen LF, Wang W. 2020. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis. Taiwan J Obstet Gynecol. 59(1):130-134.

53.   Chen CP, Hsu CY, Chern SR, Wu PS, Chen SW, Wang W. 2020. Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum. Taiwan J Obstet Gynecol. 59(1):127-129.

54.  Lee CL, Lee CH, Chuang CK, Chiu HC, Chen YJ, Chou CL, Wu PS, Chen CP, Lin HY, Lin SP. 2019. Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan. Pediatr Neonatol. 60(4):453-460.

55.   Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Chuang TY, Wang W. 2019. Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects. Taiwan J Obstet Gynecol. 58(6):869-871.

56.   Chen CP, Ko TM, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Pan CW, Wang W. 2019. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3. Taiwan J Obstet Gynecol. 58(6):864-868.

57.    Chen CP, Huang JP, Chen YY, Chern SR, Wu PS, Chen SW, Wang W, Lee CC. 2019. Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound. Taiwan J Obstet Gynecol. 58(6):859-863.

58.  Chen CP, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Wang W. 2019. Mosaic isochromosome 20q at amniocentesis: Prenatal diagnosis, genetic counseling and literature review. Taiwan J Obstet Gynecol. 58(6):855-858.

59.  Chen CP, Hung FY, Chern SR, Chen SW, Wu FT, Town DD, Wang W. 2019. Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol. 58(6):852-854.

60.   Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W. 2019. Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects. Taiwan J Obstet Gynecol. 58(5):704-708.

61.   Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W. 2019. Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization. Taiwan J Obstet Gynecol. 58(5):698-703.

62.   Chen CP, Huang MC, Chern SR, Wu PS, Chen SW, Chuang TY, Town DD, Wang W. 2019. Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review. Taiwan J Obstet Gynecol. 58(5):692-697.

63.   Chen CP, Chang SY, Lin SP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Wang W. 2018. Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1 and PAFAH1B1 in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and developmental delay. Taiwan J Obstet Gynecol. 57(5):765-768.

64.  Chen CP, Chang SY, Chen YN, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W. 2018. Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound. Taiwan J Obstet Gynecol. 57(5):739-744.

65.  Chen CP, Chang SY, Lin CJ, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Yang CW, Wang W. 2018. Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound. Taiwan J Obstet Gynecol. 57(5):734-738.

66.   Chen CP, Chang SY, Wang LK, Chang TY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Town DD, Chen LF, Wang W. 2018. Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound. Taiwan J Obstet Gynecol. 57(5):730-733.

67.   Chen CP, Lin SP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Wang W. 2018. A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows. Taiwan J Obstet Gynecol. 57(4):583-587.

68.   Chen CP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Yang CW, Wang W. 2018. Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability. Taiwan J Obstet Gynecol. 2018 Aug;57(4):578-582.

69.   Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W. 2018. Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities. Taiwan J Obstet Gynecol. 57(1):128-132.

70.   Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen LF, Wang W. 2017. Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis. Taiwan J Obstet Gynecol. 56(6):852-856.

71.  Chen CP, Hsieh CH, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W. 2017. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1. Taiwan J. Obstet. Gynecol. 56(6):847-851.

72.   Chen CP, Chang TY, Hung FY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Lee CC, Wang W. 2017. Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound. Taiwan J. Obstet. Gynecol. 56(6):843-846.

73.  Chen CP, Ko TM, Chen YY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Pan CW, Wang W. 2017. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome. Taiwan J. Obstet. Gynecol. 56(6):836-839.

74.   Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W. 2017 Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones. Taiwan J. Obstet. Gynecol. 56(6):821-826.

75.   Chen CP, Tsai C, Lin MH, Chern SR, Chen SW, Lai ST, Chen WL, Pan CW, Wang W. 2017. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism. Taiwan J. Obstet. Gynecol. 56(5):691-693.

76.   Chen CP, Huang JP, Chern SR, Chen SW, Lai ST, Wu PS, Lee CC, Yang CW, Wang W. 2017. Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwan J. Obstet. Gynecol. 56(4):569-570.

77.   Chen CP, Chen M, Wu CH, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Chang SP, Chen LF, Wang W. 2017. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review. Taiwan J. Obstet. Gynecol. 56(4):554-557.

78.   Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Lee CC, Yang CW, Wang W. 2017. Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect. Taiwan J. Obstet. Gynecol. 56(4):550-553.

79.   Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Lai ST, Yang CW, Pan CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16. Taiwan J. Obstet. Gynecol. 56(4):545-549.

80.  Chen CP, Chen M, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chang SP, Yang CW, Pan CW, Wang W. 2017. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9. Taiwan J. Obstet. Gynecol.56(4):527-533.

81.   Chen CP, Lin CJ, Chen YN, Chern SR, Chen SW, Lai ST, Wu PS, Chen LF, Wang W. 2017. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency. Taiwan J. Obstet. Gynecol. 56(3):398-401.

82.   Chen CP, Chen M, Wang PT, Chern SR, Chen SW, Lai ST, Wu PS, Chang SP, Pan CW, Wang W. 2017. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11. Taiwan J. Obstet. Gynecol. 56(3):394-397.

83.   Chen CP, Yin CS, Wang LK, Chern SR, Chen SW, Lai ST, Wu PS, Chen WL, Wang W. 2017. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome. Taiwan J. Obstet. Gynecol. 56(3):390-393.

84.   Chen CP, Yip HK, Wang LK, Chern SR, Chen SW, Lai ST, Wu PS, Wang W. 2017. Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1. Taiwan J. Obstet. Gynecol. 56(3):385-389.

85.   Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W. 2017. Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome. Taiwan J. Obstet. Gynecol. 56(2):268-269.

86.  Chen CP, Ko TM, Wang LK, Lin SP, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Town DD, Lee MS, Wang W. 2017. Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome. Taiwan J. Obstet. Gynecol. 56(2):264-267.

87.  Chen CP, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Pan CW, Yang CW, Wang W. 2017. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome. Taiwan J. Obstet. Gynecol. 56(2):238-242.

88.   Chen CP, Chen M, Chang SP, Hung FY, Lee MJ, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Chen WL, Wang W. 2017. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2. Taiwan J. Obstet. Gynecol. 56(2):234-237.

89.  Chen CP, Wang KG, Huang HK, Peng CR, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Wang W. 2017. Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis. Taiwan J. Obstet. Gynecol. 56(2):230-233.

90.  Chen CP, Chern SR, Chen YN, Chen SW, Wu PS, Yang CW, Lee CC, Lee MS, Pan CW, Wang W. 2017. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality. Taiwan J. Obstet. Gynecol. 56(2):217-223.

91.  Chen CP, Lin SP, Lee CL, Chern SR, Wu PS, Chen YN, Chen SW, Wang W. 2017. Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder. Taiwan J. Obstet. Gynecol. 56(1):98-101.

92.   Chen CP, Lin SP, Lee CL, Chern SR, Wu PS, Chen YN, Chen SW, Wang W. 2017. Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay. Taiwan J. Obstet. Gynecol. 56(1):93-97.

93.  Chen CP, Wang LK, Wu PC, Chang TY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Yang CW, Wang W. 2017. Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound. Taiwan J. Obstet. Gynecol. 56(1):102-105.

94.   Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Lee MS, Yang CW, Wang W. 2016. Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome. Taiwan J. Obstet. Gynecol. 55(6):902-903.

95.   Chen CP, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Yang CW, Wang W. 2016. Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome. Taiwan J. Obstet. Gynecol. 55(6):900-901.

96.   Chen CP, Fu CH, Lin YH, Chern SR, Wu PS, Chen YN, Chen SW, Wang W. 2016. Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality. Taiwan J Obstet. Gynecol. 55(6):871-873.

97.   Chen CP, Lin SP, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Lee MS, Wang W. 2016. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability. Taiwan J. Obstet. Gynecol. 55(6): 856-860.

98.  Chen CP, Lin SP, Lin YH, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W. 2016. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities. Taiwan J. Obstet. Gynecol. 55(6):852-855.

99.   Chen CP, Ko TM, Su YN, Wang LK, Chern SR, Wu PS, Chen YN, Chen SW, Ko K, Lee CC, Chen LF, Yang CW, Wang W. 2016. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion. Taiwan J. Obstet. Gynecol. 55(5):733-737.

100.  Chen CP, Lin SP, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Yang CW, Wang W. 2016. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome. Taiwan J. Obstet. Gynecol. 55(5):728-732.

101.  Chen CP, Wang LK, Chern SR, Chen YN, Chen SW, Wu PS, Town DD, Pan CW, Yang CW, Wang W. 2016. Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review. Taiwan J. Obstet. Gynecol. 55(5):712-717.

102. Chen CP, Chen CY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Lee MS, Yang CW, Wang W. 2016. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X) dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion. Taiwan J. Obstet. Gynecol. 55(5):705-711.

103.  Chen CP, Chang SJ, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Pan CW, Wang W. 2016. Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis. Taiwan J. Obstet. Gynecol. 55(4):602-3.

104.  Chen CP, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Chen LF, Yang CW, Wang W. 2016. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication. Taiwan J. Obstet. Gynecol. 55(4):596-601.

105.  Chen CP, Wang LK, Chern SR, Wu PS, Ko K, Chen YN, Chen SW, Lee MS, Wang W. 2016. Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly. Taiwan J. Obstet. Gynecol. 55(4):591-5.

106.  Chen CP, Chang TY, Wang LK, Chern SR, Wu PS, Chen YN, Chen SW, Chen WL, Wang W. 2016. 22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae, and congenital heart defects on prenatal ultrasound. Taiwan J Obstet Gynecol. 55(3):455-6.

107.  Chen CP, Chiang S, Wang KL, Cho FN, Chen M, Chern SR, Wu PS, Chen YN, Chen SW, Chang SP, Chen WL, Wang W. 2016. Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay. Taiwan J. Obstet. Gynecol. 55(3):419-22.

108.  Chen CP, Ko TM, Huang WC, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Pan CW, Yang CW, Wang W. 2016. Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction. Taiwan J Obstet. Gynecol. 55(3):415-8.

109.  Chen CP, Ko TM, Chern SR, Wu PS, Chen YN, Chen SW, Chen LF, Yang CW, Wang W. 2016. Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome. Taiwan J. Obstet. Gynecol. 55(2):303-4.

110.  Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Wang W. 2016. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter). Taiwan J. Obstet. Gynecol. 55(2):288-92.

111.  Chen CP, Wang YL, Chern SR, Wu PS, Chen YN, Chen SW, Chen LF, Lee MS, Yang CW, Wang W. 2016. Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes. Taiwan J. Obstet. Gynecol. 55(2):285-7.

112. Chen CP, Chen CY, Chern SR, Wu PS, Chen YN, Chen SW, Chen LF, Yang CW, Wang W. 2016. Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot. Taiwan J. Obstet. Gynecol. 55(2):270-4.

113.  Chen YN, Chen CP, Ko TM, Wang LK, Wu PC, Chang TY, Wu PS, Yang CW, Wang W. 2016. Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion. Taiwan J. Obstet. Gynecol. 55(1):117-20.

114.  Chen CP, Wang YL, Chern SR , Liu YP,Peng CR, , Kuo YL, Wu PS, Chen WL, Wang WS. 2015. Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis. Taiwan J Obstet. Gynecol. 54(1):58-61.

115.  Chen CP, Wang YL, Chern SR , Liu YP, Peng CR, Kuo YL, Wu PS, Chen WL, Wang WS. 2015. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia. Taiwan J. Obstet. Gynecol. 54(1):66-70.

116.  Chen CP, Huang MC, Chern SR , Kuo YL , Chen YN, Wu PS, Chen LF, Pan CW, Wang WS. 2015. Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature. Taiwan J. Obstet. Gynecol. 54(3):297-302.

117.  Chen CP, Chern SR, Chen YN, Wu PS, Yang CW, Chen LF, Wang W. 2015. Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review. Taiwan J. Obstet. Gynecol. 54(4):426-31.

118.  Chen CP, Lin MH, Chen YY, Chern SR, Chen YN, Wu PS, Pan CW, Lee MS, Wang W. 2015. Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haplo-insufficiency of TRPS1, RAD21 and EXT1. Taiwan J. Obstet. Gynecol. 54(4):426-31.

119.  Chen CP, Peng CR, Chang TY, Guo WY, Chen YN, Wu PS, Town DD, Wang W. 2015. Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly. Taiwan J. Obstet. Gynecol. 54(6):797-8.

120.  Chen CP, Lin SP, Chern SR, Kuo YL, Wu PS, Chen YT, Lee MS, Wang W. 2014. Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation. Gene. 535(1):88-92.

121.  Chen CP, Chen M, Chen CY, Chern SR, Wu PS, Chang SP, Kuo YL, Chen WL, Pan CW, Wang W. 2014. Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry. Gene. 536(2):425-429.

122.  Chen CP, Lin SP, Chern SR, Wu PS, Su JW, Lee CC, Wang W. 2014. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation. Taiwan J Obstet. Gynecol. 53(1):74-78.

123.  Chen CP, Lin SP, Chern SR, Wu PS, Su JW, Lee CC, Wang W. 2014. Mosaic    tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic     characterization, and literature review. Taiwan J Obstet. Gynecol. 53(1):79-85.

124.  Chen CP, Su YN, Chen SU, Chang TY, Wu PC, Chern SR, Wu PS, Kuo YL, Wang W. 2014. Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer. Taiwan J Obstet. Gynecol. 53(1):90-94.

125.  Chen CP, Wang PT, Lin SP, Chern SR, Chen YT, Wu PS, Kuo YL, Chen    WL,Wang W. 2014. Interphase FISH on uncultured amniocytes at repeat    amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes. Taiwan J Obstet. Gynecol. 53(1):100-102.

126.  Chen CP, Lin MH, Chern SR, Chen YT, Wu PS, Kuo YL, Lee MS, Wang W. 2014. Directly transmitted 4.5-Mb triplication of 4q12-q13.1: prenatal diagnosis and molecular cytogenetic characterization. Taiwan J Obstet. Gynecol. 53(1):123 -125.

127.  Chen CP, Lin CL, Ko TM, Chern SR, Chen YT, Wu PS, Kuo YL, Lee MS, Wang W. 2014. Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p. Taiwan J Obstet. Gynecol. 53(1):126-128.

128. Chen CP, Chen M, Su YN, Chern SR, Wu PS, Chang SP, Kuo YL, Chen WL,     Wang W. 2014. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15. Taiwan J Obstet. Gynecol. 53(1):129-132.

129. Kuo YL, Chen CP, Wang LK, Ko TM, Chang TY, Chern SR, Wu PS, Chen YT, Chang SY. 2014. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects. Taiwan J Obstet. Gynecol. 53(1):248-251.

130. Chen CP, Peng CR, Chern SR, Kuo YL, Wu PS, Town DD, Pan CW, Yang CW, Wang WS. 2014 . Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallistere Killian syndrome. Taiwan J Obstet. Gynecol. 53(4):566-571.

131.  Chen CP,Chen JL, Chern SR, Liu YP, Kuo YL, Chen YN, Wu PS, Town DD, Chen LF, Yang CW, Wang WS. 2014. Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2eq35.3 associated with NSD1 haploinsufficiency and Sotos syndrome. Taiwan J Obstet. Gynecol. 53(4):583-587.

132.  Chen CP, Chang YL, Chern SR, Wu PS, Su JW, Chen WL, Chen LF, Wang W. 2013. Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints. Gene 516:132-137.

133.  Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Wang W. 2013. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold. Gene 516:138-142.

134.  Chen CP, Lin CJ, Chang TY, Chern SR, Wu PS, Chen YT, Su JW, Lee CC, Chen LF, Wang W. 2013. Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization. Gene 519:164-168.

135.  Chen CP, Huang MC, Chen YY, Chern SR, Wu PS, Su JW, Town DD, Wang W. 2013. Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: Prenatal diagnosis and aCGH characterization using uncultured amniocytes. Gene 524(2):407-411

136.  Chen CP, Chang SJ, Chern SR, Wu PS, Chen YT, Su JW, Chen WL, Wang W. 2013. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1). Gene 521:311-315.

137.  Chen CP, Cheng PJ, Chang SD, Lee YX, Shih JC, Chern SR, Wu PS, Su JW, Chen YT, Hsieh AH, Chen TH, Chen LF, Wang W. 2013. Ring chromosome 21 presenting with sacrococcygeal teratoma: Prenatal diagnosis, molecular cytogenetic characterization and literature review. Gene. 522:111-116.

138.  Chen CP, Lin SP, Liu YP, Chern SR, Wu PS, Chen YT, Su JW, Lee CC, Wang W. 2013. 6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delay. Gene 523:99-102.

139.  Chen CP, Lin SP, Chern SR, Wu PS, Su JW, Wang W. 2013. A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene. Genet Couns. 24(2):243-246.

140.  Chen CP, Huang JP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Chen WL, Wang W. 2013. Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review. Gene 527:405-409.

141.  Chen CP, Huang JP, Chen YY, Chern SR, Wu PS, Su JW, Pan CW, Wang W. 2013. Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: Prenatal diagnosis and aCGH characterization using uncultured amniocytes. Gene 527:636-641.

142.  Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen WL, Wang W. 2013. Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization. Taiwan J Obstet. Gynecol. 52(2):278-284.

143.  Chen CP, Huang MC, Chern SR, Wu PS, Su JW, Wang W. 2013. Discordant anencephaly and Cantrell syndrome in monozygotic twins conceived by ICSI and IVF-ET. Taiwan J Obstet. Gynecol. 52(2):297-299.

144.  Chen CP, Hung FY, Chern SR, Wu PS, Su JW, Wang W. 2013. Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony. Taiwan J. Obstet. Gynecol. 52(2):300-302.

145.  Chen CP, Lin CJ, Chen CY, Chern SR, Wu PS, Su JW, Wang W. 2013. Maternal transmission of interstitial microdeletion in 5q13.2 detected during prenatal diagnosis of coarctation. Taiwan J. Obstet. Gynecol. 52(2):303-305.

146.  Chen CP, Tsai CH, Chern SR, Wu PS, Su JW, Lee CC, Chen YT, Chen WL, Chen LF, Wang W. 2013. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13. Gene 529(1):163-168.

147.  Chen CP, Chen M, Su YN, Huang JP, Chern SR, Wu PS, Su JW, Chang SP, Chen YT, Lee CC, Chen LF, Pan CW, Wang W. 2013. Mosaic small supernumerary marker chromosome 1 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review. Gene 529(1):169-175.

148.  Chen CP, Lin SP, Liu YP, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Wang W. 2013. An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy. Gene 529(1):176-180.

149.  Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Chen LF, Wang W. 2013. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism. Taiwan J Obstet. Gynecol. 52(3):395-400.

150.  Chen CP, Fu CH, Chern SR, Wu PS, Su JW, Lee CC, Lee MS, Wang W. 2013. De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: prenatal diagnosis and molecular cytogenetic characterization. Taiwan J Obstet. Gynecol. 52(3):401-6.

151.  Chen CP, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Pan CW, Wang W. 2013. Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis. Taiwan J Obstet. Gynecol. 52(3):450-3.

152.  Chen CP, Su YN, Chen CY, Chern SR, Wu PS, Su JW, Lee CC, Chen LF, Wang W. 2013. Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review. Genomics 102(4):265-9.

153.  Chen CP, Lee MJ, Chern SR, Wu PS, Su JW, Chen YT, Lee MS, Wang W. 2013. Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14). Gene. 529(2):351-6.

154.  Chen CP, Chang SD, Wang TH, Wang LK, Tsai JD, Liu YP, Chern SR, Wu PS, Su JW, Chen YT, Wang W. 2013. Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family. Taiwan J Obstet. Gynecol. 52(4):551-7.

155.  Chen CP, Huang MC, Chen YY, Chern SR, Wu PS, Chen YT, Su JW, Wang W. 2013. Prenatal diagnosis of de novo interstitial deletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect. Gene 531(2):496-501.

156.  Chen CP, Lin CJ, Chen YY, Wang LK, Chern SR, Wu PS, Su JW, Chen LF, Town DD, Pan CW, Wang W. 2013. 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization. Gene 532(1):80-6.

157.  Chen CP, Chang TY, Guo WY, Wu PC, Wang LK. Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Wang W. 2013. Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review. Gene 532(1):152-159.

158.  Hou P, Li Y, Zhang X, Liu C, Guan J, Li H, Zhao T, Ye J, Yang W, Liu K, Ge J, Xu J, Zhang Q, Zhao Y, Deng H. 2013. Pluripotent stem cells induced from mouse somatic cells by small molecule compounds. Science 341(6146):651-654.

159.  Chen CP, Lin S., Chern SR, Wu PS, Chang SD, Ng SH, Liu YP, Su JW , Wang W. 2012. A de novo 4.4-Mb microdeletion in 2p24.3 to 2p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome. Eu. J. Med. Genet. 55:666-669.

160.  Chen CP, Hsu CY, Chern SR, Wu PS, Su JW, Lee CC, Wang W. 2012. Rapid diagnosis of monosomy X using uncultured amniocytes in amniotic fluid and cultured lymphocytes in cystic fluid in a pregnancy with fetal cystic hygroma and hydrops. J. Med. Ultrasound. 20:129-132.

161.  Chen CP, Chen YY, Chern SR, Liou JD, Wu PS, Su JW, Lee MS. Wang W. 2012. Rapid diagnosis of trisomy 18 using uncultured amniocytes in late second trimester in a pregnancy with fetal congenital heart defects, arthrogryposis, omphalocele, and mega cistern magna. J. Med. Ultrasound. 20:186-190.

162.  Chen CP, Chen M. Chern SR, Wu PS, Chang SP, Lee DJ, Chen YT, Chen LF, Su JW, Hsieh AHR, Hsieh AHJ, Wang W. 2012. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2. Taiwan J. Obstet. Gynecol. 51:411-417.

163.  Chen CP, Su YN, Chern SR, Chen YT, Wu PS, Su JW, Pan CW, Wang W. 2012. Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis. Taiwan J Obstet. Gynecol. 51:603-611.

164.  Chen CP, Su YN, Chern SR, Wu PS, Su JW, Town DD, Wang W. 2012. Prenatal diagnosis of an interstitial deletion of 10q (10q11.21 → q21.1): array comparative genomic hybridization characterization and literature review. Taiwan J Obstet. Gynecol. 51:672-676.

165.  Chen CP, Chern SR, Wu PS, Su JW, Chen LF, Wang W. 2012. Rapid diagnosis of trisomy 21 by array comparative genomic hybridization using uncultured amniocytes in a pregnant with isolated ventriculomegaly in the fetus. J. Med. Ultrasound. 20:244-247.

166.  Chen CP, Chern SR, Chen YY, Wu PS, Town DD, Chen WL, Wang W. 2012. Monozygotic twins with trisomy 18 paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise. Taiwan J Obstet. Gynecol. 51:430-434.