Search Results - Jabareen-Masri, Azhar

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    A novel biallelic loss‐of‐function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro‐facio‐thoracic dysplasia

    A novel biallelic loss‐of‐function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro‐facio‐thoracic dysplasia by Sharkia, Rajech, Zalan, Abdelnaser, Jabareen‐Masri, Azhar, Hengel, Holger, Schöls, Ludger, Kessel, Amit, Azem, Abdussalam, Mahajnah, Muhammad

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  2. 2
    A new case confirming and expanding the phenotype spectrum of ADAT3-related intellectual disability syndrome

    A new case confirming and expanding the phenotype spectrum of ADAT3-related intellectual disability syndrome by Sharkia, Rajech, Zalan, Abdelnaser, Jabareen-Masri, Azhar, Zahalka, Hazar, Mahajnah, Muhammad

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