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Author/Creator Allam, Rabab

1. A recessive form of Marshall syndrome is caused by a mutation in the COL11A1 gene. Issue 4 (12th April 2012)

Authors:
Khalifa, Ola; Imtiaz, Faiqa; Allam, Rabab; Al-Hassnan, Zuhair; Al-Hemidan, Amal; Al-Mane, Khalid; Abuharb, Gheid; Balobaid, Ameera; Sakati, Nadia; Hyland, James; Al-Owain, Mohammed
Journal:
Journal of medical genetics
Issue:
Volume 49:Issue 4(2012)
Page Start:
246
Record Type:
Journal Article
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2. SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption. Issue 2 (February 2018)

Authors:
Al-Suyufi, Yasir; ALSaleem, Khalid; Al-Mehaidib, Ali; Banemai, Mohammed; Aldekhail, Wajeeh M.; Al-Muhandes, Abdulhakim; Mohammed, Manal; Allam, Rabab; Jambi, Amani; Ramzan, Khushnooda; Imtiaz, Faiqa
Journal:
Journal of pediatric gastroenterology and nutrition
Issue:
Volume 66:Issue 2(2018)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗