ArticleCase reports in genetics2014

A Rare, Recurrent, De Novo 14q32.2q32.31 Microdeletion of 1.1 Mb in a 20-Year-Old Female Patient with a Maternal UPD(14)-Like Phenotype and Intellectual Disability.

Almira Zada et al.PubMed ↗Full text ↗Publisher ↗

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