Search Results - Elmugadam, Abdelhakam A

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  1. 1
    A Novel Variant in the DIAPH1 Gene Causing Macrothrombocytopenia and Non-syndromic Hearing Loss in a Pediatric Saudi Girl

    A Novel Variant in the DIAPH1 Gene Causing Macrothrombocytopenia and Non-syndromic Hearing Loss in a Pediatric Saudi Girl by Alasmari, Badriah G, Alpakra, Mohammed, Hassanien, Sara S, Elmugadam, Abdelhakam A, Elzubair, Lina, Suliman, Enaam A, Alghubishi, Somayah A

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  2. 2
    LAD-III, a Mild Phenotype Resulting From a Novel Variant of FERMT3 Gene: A Case Report

    LAD-III, a Mild Phenotype Resulting From a Novel Variant of FERMT3 Gene: A Case Report by Alasmari, Badriah G, Alomari, Mohammed, Alotaibi, Wejdan N, Hommadi, Ashwaq, Elmugadam, Abdelhakam A, Abdalla, Khalid, Al-Tala, Saeed M

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    LAD-III, a Mild Phenotype Resulting From a Novel Variant of FERMT3 Gene: A Case Report

    LAD-III, a Mild Phenotype Resulting From a Novel Variant of FERMT3 Gene: A Case Report by Alasmari, Badriah G, Alomari, Mohammed, Alotaibi, Wejdan N, Hommadi, Ashwaq, Elmugadam, Abdelhakam A, Abdalla, Khalid, Al-Tala, Saeed M

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