A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies

مواد مشابهة

• Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.
  حسب: Nesbit, M, وآخرون
  منشور في: (2004)
• Molecular diagnosis of hypoparathyroidism: 2 illustrative cases
  حسب: Hampson, G, وآخرون
  منشور في: (2003)
• Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.
  حسب: Zahirieh, A, وآخرون
  منشور في: (2005)
• Clinical case seminar: Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome
  حسب: Zahirieh, A, وآخرون
  منشور في: (2005)
• A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome.
  حسب: Gaynor, K, وآخرون
  منشور في: (2009)