No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders. [electronic resource]

By: Contributor(s): Producer: 20161019Description: 283-4 p. digitalISSN:
  • 1552-4833
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 170A
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Publication Type: Letter; Research Support, Non-U.S. Gov't

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