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6. 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. Hernández AM; Villamar M; Roselló L; Moreno-Pelayo MA; Moreno F; Del Castillo I Am J Med Genet A; 2007 Apr; 143A(7):757-62. PubMed ID: 17309062 [No Abstract] [Full Text] [Related]
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17. Hypoparathyroidism, deafness, and renal dysplasia syndrome: 20 Years after the identification of the first GATA3 mutations. Lemos MC; Thakker RV Hum Mutat; 2020 Aug; 41(8):1341-1350. PubMed ID: 32442337 [TBL] [Abstract][Full Text] [Related]
18. Familial idiopathic hypoparathyroidism, sensorineural deafness and renal dysplasia. Ishida S; Isotani H; Kameoka K; Kishi T Intern Med; 2001 Feb; 40(2):110-3. PubMed ID: 11300141 [TBL] [Abstract][Full Text] [Related]
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