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Author/Creator Mohd, Howaida

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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Available online (eLD content is only available in our Reading Rooms) ↗

2. 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
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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