Showing 1 - 3 results of 3 for search 'Bronwyn Dillon', čas poizvedbe: 0.02s Refine Results
  1. 1
    First African case report of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome due to inverted duplication and deletion of chromosome 10p

    First African case report of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome due to inverted duplication and deletion of chromosome 10p od Tumelo M. Satekge, Glenrose Rikhotso, Bianca Rossouw, Bronwyn Dillon, Fiona Baine-Savanhu

    Izdano 2024-12-01
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    Article
  2. 2
    Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation

    Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation od Bronwyn Dillon, Candice Feben, David Segal, Johannes duPlessis, David Reynders, Rosalind Wainwright, Janet Poole, Amanda Krause

    Izdano 2020-08-01
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    Article
  3. 3
    Mutation analysis and clinical profile of South African patients with Neurofibromatosis type 1 (NF1) phenotype

    Mutation analysis and clinical profile of South African patients with Neurofibromatosis type 1 (NF1) phenotype od Maria Mabyalwa Mudau, Bronwyn Dillon, Clarice Smal, Candice Feben, Engela Honey, Nadia Carstens, Nadia Carstens, Amanda Krause

    Izdano 2024-03-01
    Polni tekst
    Article

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