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Author/Creator Mahmoud, Laila

1. Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience. Issue 6 (27th March 2019)

Authors:
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...
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 6(2019)
Page Start:
927
Record Type:
Journal Article
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2. Clinical genetics and genomic medicine in Qatar. Issue 5 (27th September 2018)

Authors:
Al‐Dewik, Nader; Al‐Mureikhi, Mariam; Shahbeck, Noora; Ali, Rehab; Al‐Mesaifri, Fatma; Mahmoud, Laila; Othman, Amna; AlMulla, Mariam; Sulaiman, Reem Al; Musa, Sara; Abdoh, Ghassan; El‐Akouri, Karen; Solomon, Benjamin D.; Ben‐Omran, Tawfeg
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 6:Issue 5(2018)
Page Start:
702
Record Type:
Journal Article
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3. De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder. Issue 8 (18th May 2021)

Authors:
Dias, Caroline; Pfundt, Rolph; Kleefstra, Tjitske; Shuurs‐Hoeijmakers, Janneke; Boon, Elles M. J.; van Hagen, Johanna M.; Zwijnenburg, Petra; Weiss, Marjan M.; Keren, Boris; Mignot, Cyril; Isapof, Arnaud; Weiss, Karin; Hershkovitz, Tova; Iascone, Maria; Maitz, Silvia; Feichtinger, René G.; Kotzot...
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 8(2021)
Page Start:
2384
Record Type:
Journal Article
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4. 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. Issue 1 (30th September 2021)

Authors:
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‐Om...
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 1(2022)
Page Start:
116
Record Type:
Journal Article
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5. Natural history, with clinical, biochemical, and molecular characterization of classical homocystinuria in the Qatari population. Issue 5 (8th May 2019)

Authors:
Al‐Dewik, Nader; Ali, Alaa; Mahmoud, Yassmin; Shahbeck, Noora; Ali, Rehab; Mahmoud, Laila; Al‐Mureikhi, Mariam; Al‐Mesaifri, Fatma; Musa, Sara; El‐Akouri, Karen; Almulla, Mariam; Al Saadi, Reem; Nasrallah, Gheyath K.; Samara, Muthanna; Abdoh, Ghassan; Rifai, Hilal Al; Häberle, Johannes; Thöny, Be...
Journal:
Journal of inherited metabolic disease
Issue:
Volume 42:Issue 5(2019)
Page Start:
818
Record Type:
Journal Article
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