[Spread of X-chromosome inactivation into chromosome 15 is associated with Prader Willi syndrome phenotype in a boy with a t (X ; 15) (p21.1 ; q11.2) translocation]. [electronic resource]

By: Producer: 20140618Description: 121-4 p. digitalISSN:
  • 0029-0831
Subject(s): In: No to hattatsu = Brain and development vol. 46
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Publication Type: Case Reports; Journal Article

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