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Author/Creator Mutairi, Fuad Al

1. Congenital disorders of glycosylation: The Saudi experience. Issue 10 (25th July 2017)

Authors:
Alsubhi, Sarah; Alhashem, Amal; Faqeih, Eissa; Alfadhel, Majid; Alfaifi, Abdullah; Altuwaijri, Waleed; Alsahli, Saud; Aldhalaan, Hesham; Alkuraya, Fowzan S.; Hundallah, Khalid; Mahmoud, Adel; Alasmari, Ali; Mutairi, Fuad Al; Abduraouf, Hanem; AlRasheed, Layan; Alshahwan, Saad; Tabarki, Brahim
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 10(2017)
Page Start:
2614
Record Type:
Journal Article
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3. Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing. (November 2018)

Authors:
Alfares, Ahmed; Aloraini, Taghrid; subaie, Lamia Al; Alissa, Abdulelah; Qudsi, Ahmed Al; Alahmad, Ahmed; Mutairi, Fuad Al; Alswaid, Abdulrahman; Alothaim, Ali; Eyaid, Wafaa; Albalwi, Mohammed; Alturki, Saeed; Alfadhel, Majid
Journal:
Genetics in medicine
Issue:
Volume 20:Number 11(2018)
Page Start:
1328
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗