DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndrome. [electronic resource]

By: Contributor(s): Producer: 20051114Description: 517-24 p. digitalISSN:
  • 0009-9163
Subject(s): Online resources: In: Clinical genetics vol. 66
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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