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Author/Creator Almutairi, Faten B.

1. Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new cases. (January 2018)

Authors:
Alfadhel, Majid; Nashabat, Marwan; Alrifai, Muhammad Talal; Alshaalan, Hesham; Al Mutairi, Fuad; Al-Shahrani, Saif A.; Plecko, Barbara; Almass, Rawan; Alsagob, Maysoon; Almutairi, Faten B.; Al-Rumayyan, Ahmed; Al-Twaijri, Waleed; Al-Owain, Mohammed; Taylor, Robert W.; Kaya, Namik
Journal:
European journal of paediatric neurology
Issue:
Volume 22:Number 1(2018:Jan.)
Page Start:
46
Record Type:
Journal Article
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2. Molecular and clinical spectra of FBXL4 deficiency. Issue 12 (6th October 2017)

Authors:
El‐Hattab, Ayman W.; Dai, Hongzheng; Almannai, Mohammed; Wang, Julia; Faqeih, Eissa A.; Al Asmari, Ali; Saleh, Mohammed A. M.; Elamin, Mohammed A. O.; Alfadhel, Majid; Alkuraya, Fowzan S.; Hashem, Mais; Aldosary, Mazhor S.; Almass, Rawan; Almutairi, Faten B.; Alsagob, Maysoon; Al‐Owain, Mohammed;...
Journal:
Human mutation
Issue:
Volume 38:Issue 12(2017)
Page Start:
1649
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗