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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.
Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay.
Chen CP, Chiang S, Wang KL, Cho FN, Chen M, Chern SR, Wu PS, Chen YN, Chen SW, Chang SP, Chen WL, Wang W. Chen CP, et al. Among authors: chen m, chen sw, chen yn, chen wl. Taiwan J Obstet Gynecol. 2016 Jun;55(3):419-22. doi: 10.1016/j.tjog.2016.05.002. Taiwan J Obstet Gynecol. 2016. PMID: 27343327 Free article.
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.
Chen CP, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Chen LF, Yang CW, Wang W. Chen CP, et al. Among authors: chen sw, chen yn, chen lf. Taiwan J Obstet Gynecol. 2016 Aug;55(4):596-601. doi: 10.1016/j.tjog.2016.06.008. Taiwan J Obstet Gynecol. 2016. PMID: 27590390 Free article.
1,324 results