Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13.

Source:http://linkedlifedata.com/resource/pubmed/id/9188657

Am. J. Med. Genet. 1997 Jun 13 70 3 222-8

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PMID
9188657