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Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome.
Chen CP, Lin MH, Chen YY, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Lee MS, Pan CW, Wang W. Chen CP, et al. Among authors: lin mh. Taiwan J Obstet Gynecol. 2021 Mar;60(2):335-340. doi: 10.1016/j.tjog.2021.01.012. Taiwan J Obstet Gynecol. 2021. PMID: 33678338 Free article.
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