Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations. [electronic resource]

By: Contributor(s): Producer: 20050516Description: 609-22 p. digitalISSN:
  • 0002-9297
Subject(s): Online resources: In: American journal of human genetics vol. 76
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

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