Novel mutation in the gene encoding the GATA3 transcription factor in a Spanish familial case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with female genital tract malformations. [electronic resource]

By: Contributor(s): Producer: 20071003Description: 757-62 p. digitalISSN:
  • 1552-4825
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 143A
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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