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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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主要な著者:	Chih-Ping Chen (著者), Ming-Huei Lin (著者), Yi-Yung Chen (著者), Schu-Rern Chern (著者), Peih-Shan Wu (著者), Shin-Wen Chen (著者), Fang-Tzu Wu (著者), Dai-Dyi Town (著者), Meng-Shan Lee (著者), Chen-Wen Pan (著者), Wayseen Wang (著者)
フォーマット:	図書
出版事項:	Elsevier, 2021-03-01T00:00:00Z.
主題:	article
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