Search Results - El‐Kotoury, Ahmed

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  1. 1
    Expanding the phenotypic and mutational spectrum in microcephalic osteodysplastic primordial dwarfism type I

    Expanding the phenotypic and mutational spectrum in microcephalic osteodysplastic primordial dwarfism type I by Abdel‐Salam, Ghada M.H., Abdel‐Hamid, Mohamed S., Issa, Mahmoud, Magdy, Ahmed, El‐Kotoury, Ahmed, Amr, Khalda

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  2. 2
    Mutational analysis of the PTPN11 gene in Egyptian patients with Noonan syndrome

    Mutational analysis of the PTPN11 gene in Egyptian patients with Noonan syndrome by Essawi, Mona L, Ismail, Manal F, Afifi, Hanan H, Kobesiy, Maha M, El Kotoury, Ahmed, Barakat, Maged M

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  3. 3
    Registry of ocular anomalies among patients with genetic disorders attending the clinical genetics department at the National Research Center in Egypt

    Registry of ocular anomalies among patients with genetic disorders attending the clinical genetics department at the National Research Center in Egypt by Eid, Ola M, Abdel Hady, Sawsan, El-Kotoury, Ahmed, Said, Khalda A, Rafat, Karima, El-Bassyouni, Hala T

    Published in Ophthalmic genetics
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  4. 4
    Registry of ocular anomalies among patients with genetic disorders attending the clinical genetics department at the National Research Center in Egypt

    Registry of ocular anomalies among patients with genetic disorders attending the clinical genetics department at the National Research Center in Egypt by Eid, Ola M., Abdel Hady, Sawsan, El-Kotoury, Ahmed, Said, Khalda A., Rafat, Karima, El-Bassyouni, Hala T.

    Published in Ophthalmic Genetics
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  5. 5
    Expanding the phenotypic and mutational spectrum in microcephalic osteodysplastic primordial dwarfism type I

    Expanding the phenotypic and mutational spectrum in microcephalic osteodysplastic primordial dwarfism type I by Abdel-Salam, Ghada M.H., Abdel-Hamid, Mohamed S., Issa, Mahmoud, Magdy, Ahmed, El-Kotoury, Ahmed, Amr, Khalda

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