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238 results

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First-trimester application of expanded non-invasive prenatal testing in the genetic investigation of fetal 1p36 deletion syndrome associated with a familial unbalanced reciprocal translocation of 46,XX,der(1)t(1;2) (p36.2;q37.3)dmat.
Chen CP, Weng SL, Wu FT, Wu PS, Pan YT, Chen WL, Yang CW, Wang W. Chen CP, et al. Among authors: pan yt. Taiwan J Obstet Gynecol. 2024 Nov;63(6):909-912. doi: 10.1016/j.tjog.2024.09.009. Taiwan J Obstet Gynecol. 2024. PMID: 39482002 Free article.
Rapid confirmation of trisomy 13 of maternal origin by QF-PCR following postmortem tissue cell culture failure in a pregnancy with trisomy 13 at amniocentesis and fetal postaxial polydactyly and facial cleft.
Chen CP, Chen SW, Huang JP, Chern SR, Wu FT, Pan YT, Lee CC, Wang W. Chen CP, et al. Among authors: pan yt. Taiwan J Obstet Gynecol. 2022 Nov;61(6):1048-1052. doi: 10.1016/j.tjog.2022.08.008. Taiwan J Obstet Gynecol. 2022. PMID: 36427972 Free article.
Spontaneous resolution of septated cystic hygroma with a severely increased nuchal translucency thickness of 5.8 mm detected in the first-trimester in a pregnancy with no abnormalities in chromosomal, microarray and whole exome sequencing analyses and a favorable fetal outcome.
Chen CP, Chen SW, Wu FT, Pan YT, Wang W. Chen CP, et al. Among authors: pan yt. Taiwan J Obstet Gynecol. 2022 Nov;61(6):1088-1089. doi: 10.1016/j.tjog.2022.08.010. Taiwan J Obstet Gynecol. 2022. PMID: 36427982 Free article. No abstract available.
Molecular cytogenetic characterization of de novo concomitant proximal 21q deletion of 21q11.2q21.3 and distal Xp deletion of Xp22.33p22.2 due to an unbalanced X;21 translocation detected by amniocentesis.
Chen CP, Chen SW, Wu CY, Chern SR, Wu FT, Pan YT, Wu PS, Lee CC, Chen LF, Wang W. Chen CP, et al. Among authors: pan yt. Taiwan J Obstet Gynecol. 2023 Jan;62(1):123-127. doi: 10.1016/j.tjog.2022.01.009. Taiwan J Obstet Gynecol. 2023. PMID: 36720524 Free article.
Molecular cytogenetic characterization of de novo concomitant distal 8p deletion of 8p23.3p23.1 and Xp and Xq deletion of Xp22.13q28 due to an unbalanced X;8 translocation detected by amniocentesis.
Chen CP, Hung FY, Chen SW, Wu FT, Pan YT, Wu PS, Chern SR, Lee CC, Lee MS, Wang W. Chen CP, et al. Among authors: pan yt. Taiwan J Obstet Gynecol. 2023 Jan;62(1):128-131. doi: 10.1016/j.tjog.2022.01.010. Taiwan J Obstet Gynecol. 2023. PMID: 36720525 Free article.
Mosaic 46,XY,der(15)t(6;15)(q25.1;p12)/46,XY at amniocentesis in a pregnancy associated with a favorable fetal outcome and postnatal decrease of the aneuploid cell line with the unbalanced translocation.
Chen CP, Chen SW, Chen YY, Chern SR, Wu PS, Wu FT, Pan YT, Lee CC, Chen YY, Wang W. Chen CP, et al. Among authors: pan yt. Taiwan J Obstet Gynecol. 2023 Jan;62(1):142-147. doi: 10.1016/j.tjog.2022.01.013. Taiwan J Obstet Gynecol. 2023. PMID: 36720528 Free article.
Mosaic tetrasomy 9p at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy in various tissues.
Chen CP, Chen SW, Chern SR, Wu PS, Wu FT, Pan YT, Lee CC, Pan CW, Chen YY, Wang W. Chen CP, et al. Among authors: pan yt, pan cw. Taiwan J Obstet Gynecol. 2023 Jan;62(1):148-154. doi: 10.1016/j.tjog.2022.01.014. Taiwan J Obstet Gynecol. 2023. PMID: 36720529 Free article.
238 results