Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience
Al‐Dewik, Nader, Mohd, Howaida, Al‐Mureikhi, Mariam, Ali, Rehab, Al‐Mesaifri, Fatma, Mahmoud, Laila, Shahbeck, Noora, El‐Akouri, Karen, Almulla, Mariam, Al Sulaiman, Reem, Musa, Sara, Al‐Marri, Ajayeb Al‐Nabet, Richard, Gabriele, Juusola, Jane, Solomon, Benjamin D., Alkuraya, Fowzan S., Ben‐Omran, Tawfeg
Published in American journal of medical genetics. Part A (01.06.2019)
Published in American journal of medical genetics. Part A (01.06.2019)
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Journal Article
Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in DCAF17: Report of 58 additional patients from Qatar and literature review
Ali, Rehab, Al‐Dewik, Nader, Mohammed, Shayma, Elfituri, Mahmud, Agouba, Sahar, Musa, Sara, Mahmoud, Laila, Almulla, Mariam, El‐Akouri, Karen, Mohd, Howaida, Bux, Reem, Almulla, Hajer, Othman, Amna, Al‐Mesaifri, Fatma, Shahbeck, Noora, Al‐Muriekhi, Mariam, Khalifa, Amal, Al‐Sulaiman, Reem, Ben‐Omran, Tawfeg
Published in American journal of medical genetics. Part A (01.01.2022)
Published in American journal of medical genetics. Part A (01.01.2022)
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Journal Article