Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss. [electronic resource]

By: Contributor(s): Producer: 20070409Description: 385-6 p. digitalISSN:
  • 1552-4825
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 143
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Publication Type: Journal Article; Research Support, N.I.H., Extramural

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