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

Παρόμοια τεκμήρια

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