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Author/Creator Al‐Sulaiman, Reem

1. A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families. Issue 11 (28th August 2020)

Authors:
Al‐Sulaiman, Reem; Othman, Amna; El‐Akouri, Karen; Fareed, Shehab; AlMulla, Hajer; Sukik, Aseel; Al‐Mureikhi, Mariam; Shahbeck, Noora; Ali, Rehab; Al‐Mesaifri, Fatma; Musa, Sara; Al‐Mulla, Mariam; Ibrahim, Khalid; Mohamed, Khalid; Al‐Nesef, Maryam Ali; Ehlayel, Mohammad; Ben‐Omran, Tawfeg
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 11(2020)
Page Start:
2570
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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