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Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay

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Description scientific article published in February 2017
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author: Chih-Ping Chen  Schu-Rern Chern  Wayseen Wang  Peih-Shan Wu  Shin-Wen Chen  Shuan-Pei Lin 

Publication date February 1, 2017
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