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

समान संसाधन

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