Recurrent mutation in CDMP1 in a family with Grebe chondrodysplasia: broadening the phenotypic manifestation of syndrome in Pakistani population. [electronic resource]

By: Contributor(s): Producer: 20160212Description: 1542-4 p. digitalISSN:
  • 1682-024X
Online resources: In: Pakistan journal of medical sciences vol. 31
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Publication Type: Case Reports; Journal Article

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