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Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome.

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author: Chih-Ping Chen  Kai-Liang Wang  Schu-Rern Chern  Dai-Dyi Town  Wayseen Wang  Peih-Shan Wu  Shin-Wen Chen  Chien-Wen Yang  Meng-Shan Lee  Shuan-Pei Lin 

Publication date April 1, 2017
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