Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

Éric Bieth(Hôpital Purpan), M. Tauber(Centre National de la Recherche Scientifique)
European Journal of Human Genetics
June 11, 2014
10.1038/ejhg.2014.103
Cited by 179

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