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Low-level mosaic trisomy 21 due to mosaic unbalanced Robertsonian translocation of 46,XX,+21,der(21;21) (q10;q10)/46,XX at amniocentesis in a pregnancy associated with a favorable fetal outcome, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, cytogenetic discrepancy among various tissues and perinatal progressive decrease of the trisomy 21 cell line.
Chen CP, Chen YY, Wu FT, Pan YT, Lee CC, Wang W. Chen CP, et al. Among authors: pan yt. Taiwan J Obstet Gynecol. 2024 Nov;63(6):931-934. doi: 10.1016/j.tjog.2024.09.014. Taiwan J Obstet Gynecol. 2024. PMID: 39482007
Prenatal diagnosis of Jacobsen syndrome associated with a distal 11q deletion and a distal 8q duplication by chromosome microarray analysis in a fetus with a de novo unbalanced translocation of 46,XX,der(11)t(8;11)(q24.13;q23.3) and multiple congenital anomalies on fetal ultrasound.
Chen CP, Huang JP, Wu FT, Wu PS, Pan YT, Lee CC, Chen WL, Wang W. Chen CP, et al. Among authors: pan yt. Taiwan J Obstet Gynecol. 2024 Nov;63(6):922-926. doi: 10.1016/j.tjog.2024.09.012. Taiwan J Obstet Gynecol. 2024. PMID: 39482005
Detection of chromosome 5q interstitial deletion of 5q14.3-q31.1 by chromosome microarray analysis in a second-trimester fetus with multiple congenital anomalies and a literature review of chromosome 5q interstitial deletion syndrome.
Chen CP, Huang JP, Wu FT, Wu PS, Pan YT, Wang W. Chen CP, et al. Among authors: pan yt. Taiwan J Obstet Gynecol. 2024 Nov;63(6):918-921. doi: 10.1016/j.tjog.2024.09.011. Taiwan J Obstet Gynecol. 2024. PMID: 39482004 Review.
Prenatal diagnosis of a 14-Mb 11p11.2-p13 deletion by chromosome microarray analysis in a pregnancy with fetal recombinant chromosome 11 syndrome of rec(11)del(11)(p11.2p13)ins(11)(q21p11.2p13) and maternal intrachromosomal insertion of ins(11)(q21p11.2p13).
Chen CP, Chen CY, Wu FT, Wu PS, Pan YT, Lee CC, Chen WL, Wang W. Chen CP, et al. Among authors: pan yt. Taiwan J Obstet Gynecol. 2024 Nov;63(6):913-917. doi: 10.1016/j.tjog.2024.09.010. Taiwan J Obstet Gynecol. 2024. PMID: 39482003
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
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