Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 372

1.

Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects.

Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2019 Sep;58(5):704-708. doi: 10.1016/j.tjog.2019.07.022.

2.

Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization.

Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2019 Sep;58(5):698-703. doi: 10.1016/j.tjog.2019.07.021.

3.

Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review.

Chen CP, Huang MC, Chern SR, Wu PS, Chen SW, Chuang TY, Town DD, Wang W.

Taiwan J Obstet Gynecol. 2019 Sep;58(5):692-697. doi: 10.1016/j.tjog.2019.07.020.

4.

Digynic triploidy in a fetus presenting with semilobar holoprosencephaly.

Chuang TY, Chang SY, Chen CP, Lin MH, Chen CY, Chen SW, Chern SR, Lee CC, Town DD, Wang W.

Taiwan J Obstet Gynecol. 2018 Dec;57(6):881-884. doi: 10.1016/j.tjog.2018.11.001.

5.

Characterization of the Genome Sequences of Enterovirus C109 from Two Respiratory Disease Cases in Florida, 2016.

Ng TFF, Yglesias JA, Stevenson-Yuen TA, Wolfe CM, Cone MR, Heberlein-Larson LA, Maher K, Rogers S, Chern SW, Montmayeur A, Castro C, Nix WA.

Microbiol Resour Announc. 2018 Jul 26;7(3). pii: e00803-18. doi: 10.1128/MRA.00803-18. eCollection 2018 Jul.

6.

Detection of hypomethylation of H19 in a pregnancy with limb-body wall complex.

Chen CP, Chang SY, Huang MC, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):769-771. doi: 10.1016/j.tjog.2018.08.032. No abstract available.

7.

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.

Chen CP, Chang SY, Lin SP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):765-768. doi: 10.1016/j.tjog.2018.08.031. No abstract available.

8.

Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.

Chen CP, Chang SY, Chen YN, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):739-744. doi: 10.1016/j.tjog.2018.08.024.

9.

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.

Chen CP, Chang SY, Lin CJ, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):734-738. doi: 10.1016/j.tjog.2018.08.023.

10.

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.

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.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):730-733. doi: 10.1016/j.tjog.2018.08.022.

11.

A 17-year-old boy with Klinefelter syndrome presenting Marfan syndrome-like clinical features of tall stature, scoliosis, arachnodactyly and subluxation of bilateral elbow joints.

Chen CP, Lin SP, Chern SR, Chen SW, Lai ST, Chuang TY, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2018 Aug;57(4):608-610. doi: 10.1016/j.tjog.2018.06.025. No abstract available.

12.

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.

Chen CP, Lin SP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2018 Aug;57(4):583-587. doi: 10.1016/j.tjog.2018.06.019.

13.

Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability.

Chen CP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2018 Aug;57(4):578-582. doi: 10.1016/j.tjog.2018.06.018.

14.

Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities.

Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2018 Feb;57(1):128-132. doi: 10.1016/j.tjog.2017.12.022.

15.

Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus.

Chen CP, Ko TM, Chang TY, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W.

Taiwan J Obstet Gynecol. 2018 Feb;57(1):123-127. doi: 10.1016/j.tjog.2017.12.021.

16.

Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia.

Chen CP, Chang TY, Lin TW, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W.

Taiwan J Obstet Gynecol. 2018 Feb;57(1):119-122. doi: 10.1016/j.tjog.2017.12.020. Review.

17.

Uterine fibroid or ovarian fibroma: importance of comprehensive preoperative consent-taking to include unexpected findings with management implications.

Kwek LK, Wee-Stekly WW, Chern SMB.

BMJ Case Rep. 2018 Feb 7;2018. pii: bcr-2017-222608. doi: 10.1136/bcr-2017-222608.

PMID:
29437720
18.

Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis.

Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):852-856. doi: 10.1016/j.tjog.2017.10.034.

19.

Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1.

Chen CP, Hsieh CH, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):847-851. doi: 10.1016/j.tjog.2017.10.027.

20.

Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound.

Chen CP, Chang TY, Hung FY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):843-846. doi: 10.1016/j.tjog.2017.10.026.

21.

Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome.

Chen CP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):840-842. doi: 10.1016/j.tjog.2017.10.025.

22.

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.

Chen CP, Ko TM, Chen YY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):836-839. doi: 10.1016/j.tjog.2017.10.024.

23.

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.

Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):821-826. doi: 10.1016/j.tjog.2017.10.021.

24.

Severe Respiratory Illness Associated With Rhinovirus During the Enterovirus D68 Outbreak in the United States, August 2014-November 2014.

Prill MM, Dahl RM, Midgley CM, Chern SW, Lu X, Feikin DR, Sakthivel SK, Nix WA, Watson JT, Gerber SI, Oberste MS.

Clin Infect Dis. 2018 May 2;66(10):1528-1534. doi: 10.1093/cid/cix1034.

PMID:
29186347
25.

Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.

Chen CP, Tsai C, Lin MH, Chern SR, Chen SW, Lai ST, Chen WL, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Oct;56(5):691-693. doi: 10.1016/j.tjog.2017.09.001.

26.

Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome.

Chen CP, Huang JP, Chern SR, Chen SW, Lai ST, Wu PS, Lee CC, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):569-570. doi: 10.1016/j.tjog.2017.05.007. No abstract available.

27.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21.

Chen CP, Chen M, Chern SR, Chang SP, Chen SW, Lai ST, Chen WL, Lee MS, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):566-568. doi: 10.1016/j.tjog.2017.05.006. No abstract available.

28.

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.

Chen CP, Chen M, Wu CH, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Chang SP, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):554-557. doi: 10.1016/j.tjog.2017.06.004. Review.

29.

Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect.

Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Lee CC, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):550-553. doi: 10.1016/j.tjog.2017.06.003.

30.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.

Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Lai ST, Yang CW, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):545-549. doi: 10.1016/j.tjog.2017.05.004.

31.

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.

Chen CP, Chen M, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chang SP, Yang CW, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):527-533. doi: 10.1016/j.tjog.2017.06.002.

32.

Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia.

Chen CP, Lin SP, Liu YP, Chern SR, Chen SW, Lai ST, Wang W.

Taiwan J Obstet Gynecol. 2017 Jun;56(3):412-414. doi: 10.1016/j.tjog.2017.04.030. No abstract available.

33.
34.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11.

Chen CP, Chen M, Wang PT, Chern SR, Chen SW, Lai ST, Wu PS, Chang SP, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Jun;56(3):394-397. doi: 10.1016/j.tjog.2017.04.025.

35.

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.

Chen CP, Yin CS, Wang LK, Chern SR, Chen SW, Lai ST, Wu PS, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2017 Jun;56(3):390-393. doi: 10.1016/j.tjog.2017.04.024.

36.
37.

Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome.

Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2017 Apr;56(2):268-269. doi: 10.1016/j.tjog.2017.01.007. No abstract available.

38.

Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome.

Chen CP, Ko TM, Wang LK, Lin SP, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Town DD, Lee MS, Wang W.

Taiwan J Obstet Gynecol. 2017 Apr;56(2):264-267. doi: 10.1016/j.tjog.2017.01.006. No abstract available.

39.

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome.

Chen CP, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Pan CW, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Apr;56(2):238-242. doi: 10.1016/j.tjog.2017.01.005.

40.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2.

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.

Taiwan J Obstet Gynecol. 2017 Apr;56(2):234-237. doi: 10.1016/j.tjog.2017.01.004.

41.

Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis.

Chen CP, Wang KG, Huang HK, Peng CR, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2017 Apr;56(2):230-233. doi: 10.1016/j.tjog.2017.01.003.

42.

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.

Chen CP, Chern SR, Chen YN, Chen SW, Wu PS, Yang CW, Lee CC, Lee MS, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Apr;56(2):217-223. doi: 10.1016/j.tjog.2017.01.002.

43.

Enterovirus D68 Infection Among Children With Medically Attended Acute Respiratory Illness, Cincinnati, Ohio, July-October 2014.

Biggs HM, McNeal M, Nix WA, Kercsmar C, Curns AT, Connelly B, Rice M, Chern SW, Prill MM, Back N, Oberste MS, Gerber SI, Staat MA.

Clin Infect Dis. 2017 Jul 15;65(2):315-323. doi: 10.1093/cid/cix314.

44.

Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder.

Chen CP, Lin SP, Lee CL, Chern SR, Wu PS, Chen YN, Chen SW, Wang W.

Taiwan J Obstet Gynecol. 2017 Feb;56(1):98-101. doi: 10.1016/j.tjog.2016.12.003.

45.

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.

Chen CP, Lin SP, Lee CL, Chern SR, Wu PS, Chen YN, Chen SW, Wang W.

Taiwan J Obstet Gynecol. 2017 Feb;56(1):93-97. doi: 10.1016/j.tjog.2016.12.002.

46.

Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3.

Chen SW, Chen CP, Wang LK, Chern SR, Wu PC, Chen YN, Lin CJ, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2017 Feb;56(1):87-92. doi: 10.1016/j.tjog.2016.12.013.

47.

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.

Chen CP, Wang LK, Wu PC, Chang TY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Feb;56(1):102-105. doi: 10.1016/j.tjog.2016.12.004.

48.

Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome.

Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Lee MS, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2016 Dec;55(6):902-903. doi: 10.1016/j.tjog.2016.10.001. No abstract available.

49.

Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome.

Chen CP, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2016 Dec;55(6):900-901. doi: 10.1016/j.tjog.2016.08.006. No abstract available.

50.

Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling.

Chen CP, Chern SR, Chiu NC, Liu YP, Chen YN, Chen SW, Wang W.

Taiwan J Obstet Gynecol. 2016 Dec;55(6):897-899. doi: 10.1016/j.tjog.2016.08.005. No abstract available.

Supplemental Content

Support Center