Search Results - C Feben

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  1. 1

    Case Report: FBN1 mutation screening in South African patients with Marfan syndrome by F. Mhlongo, C. Feben, A. Krause, N. Carstens, N. Carstens

    Published in Frontiers in Genetics (2025-07-01)
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  2. 2

    Fanconi Anaemia in South African Patients with Afrikaner Ancestry by C Feben, T Haw, D Stones, C Jacobs, C Sutton, J Kromberg, A Krause

    Published in South African Journal of Child Health (2017-10-01)
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