Search Results - Bdier, A.Y.

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  1. 1
    De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome

    De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome by Al-Aama, J.Y., Al-Ghamdi, S., Bdier, A.Y., Wilde, A.A.M., Bhuiyan, Zahurul A.

    Published in Clinical genetics
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  2. 2
    Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia

    Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia by Al-Aama, J.Y., Al-Ghamdi, S., Bdier, A.Y., AlQarawi, A., Jiman, O.A., Al-Aama, N., Al-Aata, J., Wilde, A.A.M., Bhuiyan, Z.A.

    Published in Clinical genetics
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