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Author/Creator Alhashemi, Nadia

1. Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype. Issue 4 (22nd March 2017)

Authors:
Altassan, Ruqaiah; Saud, Haya Al; Masoodi, Tariq Ahmad; Dosssari, Haya Al; Khalifa, Ola; Al‐Zaidan, Hamad; Sakati, Nadia; Rhabeeni, Zuhair; Al‐Hassnan, Zuhair; Binamer, Yousef; Alhashemi, Nadia; Wade, William; Al‐Zayed, Zayed; Al‐Sayed, Moeen; Al‐Muhaizea, Mohamed A.; Meyer, Brian; Al‐Owain, Moha...
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 4(2017)
Page Start:
1009
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. The many faces of peroxisomal disorders: Lessons from a large Arab cohort. Issue 2 (18th December 2018)

Authors:
Alshenaifi, Jumanah; Ewida, Nour; Anazi, Shams; Shamseldin, Hanan E.; Patel, Nisha; Maddirevula, Sateesh; Al‐Sheddi, Tarfa; Alomar, Rana; Alobeid, Eman; Ibrahim, Niema; Hashem, Mais; Abdulwahab, Firdous; Jacob, Minnie; Alhashem, Amal; Alzaidan, Hamad I.; Seidahmed, Mohammed Z.; Alhashemi, Nadia; ...
Journal:
Clinical genetics
Issue:
Volume 95:Issue 2(2019)
Page Start:
310
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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