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

Samankaltaisia teoksia

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