Showing 1 - 2 results of 2 for search 'Zahirieh, A', query time: 0.02s Refine Results
  1. 1
    Clinical case seminar: Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome

    Clinical case seminar: Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome by Zahirieh, A, Nesbit, M, Ali, A, Wang, K, He, N, Stangou, M, Bamichas, G, Sombolos, K, Thakker, R, Pei, Y

    Published 2005
    Journal article
  2. 2
    Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.

    Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome. by Zahirieh, A, Nesbit, M, Ali, A, Wang, K, He, N, Stangou, M, Bamichas, G, Sombolos, K, Thakker, R, Pei, Y

    Published 2005
    Journal article

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