Author/Creator: Alshehri, Meshal - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Alshehri, Meshal

1. A homozygous loss-of-function mutation in GP1BB causing variable clinical phenotypes in a family with Bernard–Soulier syndrome. Issue 5 (July 2021)

Authors:: Al-Numair, Nouf; Ramzan, Khushnooda; Alquait, Laila; Alshehri, Meshal; Imtiaz, Faiqa; Owaidah, Tarek
Journal:: Blood coagulation and fibrinolysis
Issue:: Volume 32:Issue 5(2021)
Page Start:
Record Type:: Journal Article
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2. LCR based quick detection of hotspot G1896A mutation in patients with different spectrum of hepatitis B. Issue 5 (May 2021)

Authors:: Malik, Abdul; Aldakheel, Fahad; Rabbani, Syed; Alshehri, Meshal; Chaudhary, Anis Ahmad; Alkholief, Musaed; Alshamsan, Aws
Journal:: Journal of infection and public health
Issue:: Volume 14:Issue 5(2021)
Page Start:: 651
Record Type:: Journal Article
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