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Am J Med Genet A. 2007 Apr 1;143A(7):757-62.

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.

Author information

1
Unidad de Genética Molecular, Hospital Ramón y Cajal, Madrid, Spain.
PMID:
17309062
DOI:
10.1002/ajmg.a.31617
[Indexed for MEDLINE]

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