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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.
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.
Chen CP, Su YN, Chen YY, Chern SR, Liu YP, Wu PC, Lee CC, Chen YT, Wang W. Chen CP, et al. Among authors: chen yy, chen yt. Taiwan J Obstet Gynecol. 2011 Sep;50(3):345-52. doi: 10.1016/j.tjog.2011.07.014. Taiwan J Obstet Gynecol. 2011. PMID: 22030051 Free article.
Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
Chen CP, Su YN, Chen YY, Su JW, Chern SR, Chen YT, Chen WL, Chen LF, Wang W. Chen CP, et al. Among authors: chen yy, chen wl, chen lf, chen yt. Taiwan J Obstet Gynecol. 2011 Dec;50(4):506-11. doi: 10.1016/j.tjog.2011.10.019. Taiwan J Obstet Gynecol. 2011. PMID: 22212326 Free article.
4,338 results