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

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

Objective: We present prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency (NT), mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter, and Prader–Willi syndrome (PWS). Case report: A 32-...

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Bibliographic Details
Main Authors:	Chih-Ping Chen, Ming-Huei Lin, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang
Format:	Article
Language:	English
Published:	Elsevier 2021-03-01
Series:	Taiwanese Journal of Obstetrics & Gynecology
Subjects:	15q11-q14 deletion Mosaicism Prader–Willi syndrome Prenatal diagnosis Unbalanced translocation
Online Access:	http://www.sciencedirect.com/science/article/pii/S1028455921000127

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