Missense and deletion mutations in GJA1 causing oculodentodigital dysplasia in two Indian families. [electronic resource]

By: Contributor(s): Producer: 20160620Description: 159-62 p. digitalISSN:
  • 1473-5717
Subject(s): Online resources: In: Clinical dysmorphology vol. 24
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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