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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

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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Main Authors:	Chih-Ping Chen (Author), Ming-Huei Lin (Author), Yi-Yung Chen (Author), Schu-Rern Chern (Author), Peih-Shan Wu (Author), Shin-Wen Chen (Author), Fang-Tzu Wu (Author), Dai-Dyi Town (Author), Meng-Shan Lee (Author), Chen-Wen Pan (Author), Wayseen Wang (Author)
Format:	Book
Published:	Elsevier, 2021-03-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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