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Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency.

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Description scientific article published in June 2017
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author: Chih-Ping Chen  Schu-Rern Chern  Wayseen Wang  Peih-Shan Wu  Shin-Wen Chen  Shih-Ting Lai 

Publication date June 1, 2017
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