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Hemoglobin|August 7, 2009
A novel deletional beta-thalassemic variant in an ethnic Qatari patientAisha Al-Obaidli, Nathalie Gerard, Shoaib Al Zadjali, et al.Oman Medical Journal|May 19, 2026
Antiviral Therapy and Hepatitis B Reactivation Outcomes in Chronic Myeloid Leukemia Treated with Tyrosine Kinase Inhibitors: A Retrospective Cohort StudySalam Al Kindi, Shahla S Al-Jabri, Anil Pathare, et al.Medicine International|April 1, 2025
Next‑generation sequencing failure rates in rare tumors: A real‑world single‑institution analysisBoris Itkin, Prashant Ajit Deshpande, Anoopa Pullanhi, et al.Frontiers in Medicine|February 25, 2025
Case report: A novel 11-bp deletion in exon 11 causing a frameshift in the C-terminal of the <i>ALAS2</i> gene leading to X-linked sideroblastic anemia-a family studySalam Al Kindi, Altaf Al-Mamari, Shoaib Al-Zadjali, et al.Cancers|January 11, 2024
Deciphering Urogenital Cancers through Proteomic Biomarkers: A Systematic Review and Meta-AnalysisAafaque Ahmad Khan, Nahad Al-Mahrouqi, Aida Al-Yahyaee, et al.European Journal of Haematology|August 2, 2011
The β-globin promoter -71 C>T mutation is a β+ thalassemic alleleShoaib Al Zadjali, Yasser Wali, Fatma Al Lawatiya, et al.Journal of Clinical Pathology|August 9, 2017
Haemoglobin Fontainebleau (HBA2: c. 64G>C) in Oman: molecular and haematological characteristics and interaction with various haemoglobinopathiesShahina Daar, Shoaib Al Zadjali, Salam Alkindi, et al.Journal of Human Genetics|August 3, 2012
Warfarin pharmacogenetics: development of a dosing algorithm for Omani patientsAnil Pathare, Murtadha Al Khabori, Salam Alkindi, et al.Hemoglobin|February 6, 2020
α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean RegionArwa Z Al-Riyami, Shahina Daar, Salam Al Kindi, et al.Hemoglobin|March 23, 2011
Hb A2' (Hb B2) in the Omani population and diagnostic significanceShahina Daar, Shoaib Al Zadjali, David Gravell, et al.Pageof 4