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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. Chen CP, et al. Among authors: chen m, chen sw, chen yn, chen lf. Taiwan J Obstet Gynecol. 2017 Aug;56(4):554-557. doi: 10.1016/j.tjog.2017.06.004. Taiwan J Obstet Gynecol. 2017. PMID: 28805618 Free article. Review.
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 haploinsufficiency of TRPS1, RAD21 and EXT1.
Chen CP, Lin MH, Chen YY, Chern SR, Chen YN, Wu PS, Pan CW, Lee MS, Wang W. Chen CP, et al. Among authors: chen yy, chen yn. Taiwan J Obstet Gynecol. 2015 Oct;54(5):592-6. doi: 10.1016/j.tjog.2015.08.013. Taiwan J Obstet Gynecol. 2015. PMID: 26522117 Free article.
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.
Chen CP, Peng CR, Chang TY, Guo WY, Chen YN, Wu PS, Town DD, Wang W. Chen CP, et al. Among authors: chen yn. Taiwan J Obstet Gynecol. 2015 Dec;54(6):797-8. doi: 10.1016/j.tjog.2015.10.023. Taiwan J Obstet Gynecol. 2015. PMID: 26701010 Free article. No abstract available.
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.
Chen CP, Chen CY, Chern SR, Wu PS, Chen YN, Chen SW, Chen LF, Yang CW, Wang W. Chen CP, et al. Among authors: chen sw, chen yn, chen cy, chen lf. Taiwan J Obstet Gynecol. 2016 Apr;55(2):270-4. doi: 10.1016/j.tjog.2016.02.013. Taiwan J Obstet Gynecol. 2016. PMID: 27125413 Free article.
614 results