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Author/Creator Alasmari, Ali

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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2. El‐Hattab‐Alkuraya syndrome caused by biallelic WDR45B pathogenic variants: Further delineation of the phenotype and genotype. Issue 5 (12th April 2022)

Authors:
Almannai, Mohammed; Marafi, Dana; Abdel‐Salam, Ghada M. H.; Zaki, Maha S.; Duan, Ruizhi; Calame, Daniel; Herman, Isabella; Levesque, Felix; Elbendary, Hasnaa M.; Hegazy, Ibrahim; Chung, Wendy K.; Kavus, Haluk; Saeidi, Kolsoum; Maroofian, Reza; AlHashim, Aqeela; Al‐Otaibi, Ali; Al Madhi, Asma; Abo...
Journal:
Clinical genetics
Issue:
Volume 101:Issue 5/6(2022)
Page Start:
530
Record Type:
Journal Article
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3. Expanded Newborn Screening Program in Saudi Arabia: Incidence of screened disorders. (24th March 2017)

Authors:
Alfadhel, Majid; Al Othaim, Ali; Al Saif, Saif; Al Mutairi, Fuad; Alsayed, Moeenaldeen; Rahbeeni, Zuhair; Alzaidan, Hamad; Alowain, Mohammed; Al‐Hassnan, Zuhair; Saeedi, Mohamad; Aljohery, Saeed; Alasmari, Ali; Faqeih, Eissa; Alwakeel, Mansour; AlMashary, Maher; Almohameed, Sulaiman; Alzahrani, M...
Journal:
Journal of paediatrics and child health
Issue:
Volume 53:Number 6(2017:Jun.)
Page Start:
585
Record Type:
Journal Article
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