Search Results - Ahlam A. Hamed

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  1. 1
    Bi-allelic variants in<i>WDR47</i>lead to neuronal loss causing a rare neurodevelopmental syndrome with corpus callosum dysgenesis in humans

    Bi-allelic variants in<i>WDR47</i>lead to neuronal loss causing a rare neurodevelopmental syndrome with corpus callosum dysgenesis in humans by Efil Bayam, Peggy Tilly, Stephan C. Collins, José Rivera Alvarez, Meghna Kannan, Lucile Tonneau, Bruno Rinaldi, Romain Lecat, Noémie Schwaller, Sateesh Maddirevula, Fabíola Paoli Monteiro, João Paulo Kitajima, Fernando Kok, Mitsuhiro Kato, Ahlam A. Hamed, Mustafa A. Salih, Saeed Al Tala, Mais Hashem, Hiroko Tada, Hirotomo Saitsu, Sylvie Friant, Zafer Yüksel, Mitsuko Nakashima, Fowzan S. Alkuraya, Binnaz Yalcin, Juliette D. Godin

    Published 2023
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    Expanding the phenome and variome of skeletal dysplasia

    Expanding the phenome and variome of skeletal dysplasia by Sateesh Maddirevula, Saud Alsahli, Lamees Alhabeeb, Nisha Patel, Fatema Alzahrani, Hanan E. Shamseldin, Shams Anazi, Nour Ewida, Hessa S. Alsaif, Jawahir Y. Mohamed, Anas M. Alazami, Niema Ibrahim, Firdous Abdulwahab, Mais Hashem, Mohamed Abouelhoda, Dorota Monies, Nada Al Tassan, Muneera J. Alshammari, Afaf Alsagheir, Mohammed Zain Seidahmed, Samira Sogati, Mona Aglan, Muddathir H. Hamad, Mustafa A. Salih, Ahlam A. Hamed, Nadia Alhashmi, Amira Nabil, Fatima Alfadli, Ghada M. H. Abdel‐Salam, Hisham Alkuraya, Winnie Ong Peitee, Wee Teik Keng, Abdullah Qasem, Aziza Mushiba, Maha S. Zaki, Mahmoud R. Fassad, Majid Alfadhel, Saji Alexander, Yasser Sabr, Samia A. Temtamy, Alka V. Ekbote, Samira Ismail, Gamal Ahmed Hosny, Ghada A. Otaify, Khalda Amr, Saeed Al Tala, Arif O. Khan, Tamer Rizk, Aida I. Al‐Aqeel, Abdulmonem Alsiddiky, Ankur Singh, Seema Kapoor, Amal Alhashem, Eissa Faqeih, Ranad Shaheen, Fowzan S. Alkuraya

    Published 2018
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