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Fetal blood sampling and cytogenetic abnormalities.
Liou JD, Chen CP, Breg WR, Hobbins JC, Mahoney MJ, Yang-Feng TL. Liou JD, et al. Prenat Diagn. 1993 Jan;13(1):1-8. doi: 10.1002/pd.1970130102. Prenat Diagn. 1993. PMID: 8446566
Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.
Chen CP, Liou JD, Chern SR, Wu PS, Chen SW, Wu FT, Lee MS, Chen YY, Wang W. Chen CP, et al. Among authors: liou jd. Taiwan J Obstet Gynecol. 2022 Jan;61(1):146-149. doi: 10.1016/j.tjog.2021.11.025. Taiwan J Obstet Gynecol. 2022. PMID: 35181027 Free article.
Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results.
Chen CP, Liou JD, Seow KM, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Chen LF, Wang W. Chen CP, et al. Among authors: liou jd. Taiwan J Obstet Gynecol. 2020 Sep;59(5):758-762. doi: 10.1016/j.tjog.2020.07.024. Taiwan J Obstet Gynecol. 2020. PMID: 32917332 Free article.
46 results