Shoaib Al Zadjali

Muscat, MA 123, Oman

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 17 publications

Next‑generation sequencing failure rates in rare tumors: A real‑world single‑institution analysis.

Next‑generation sequencing failure rates in rare tumors: A real‑world single‑institution analysis.

Journal: Medicine international

Published: October 07, 2024

Mortality and complications in Omani patients with beta-thalassemia major: a long-term follow-up study.

Mortality and complications in Omani patients with beta-thalassemia major: a long-term follow-up study.

Journal: Acta bio-medica : Atenei Parmensis

Published: June 03, 2023

IDH1 and IDH2 Gene Mutations in Omani Patients with Acute Myeloid Leukemia: Prognostic Significance and Clinic-pathologic Features.

IDH1 and IDH2 Gene Mutations in Omani Patients with Acute Myeloid Leukemia: Prognostic Significance and Clinic-pathologic Features.

Journal: Oman medical journal

Published: August 15, 2022

Cardio-protective effect of regular transfusion in children with non-transfusion dependent thalassemia (NTDT): A cohort study.

Cardio-protective effect of regular transfusion in children with non-transfusion dependent thalassemia (NTDT): A cohort study.

Journal: Acta bio-medica : Atenei Parmensis

Published: October 22, 2020

Clinical and Laboratory Features of Hemoglobin La Desirade Variant in Association with Sickle Cell and Alpha Thalassemia Genes.

Clinical and Laboratory Features of Hemoglobin La Desirade Variant in Association with Sickle Cell and Alpha Thalassemia Genes.

Journal: Mediterranean journal of hematology and infectious diseases

Published: September 18, 2020

The Use of HPLC as a Tool for Neonatal Cord Blood Screening of haemoglobinopathy: A Validation Study.

The Use of HPLC as a Tool for Neonatal Cord Blood Screening of haemoglobinopathy: A Validation Study.

Journal: Mediterranean journal of hematology and infectious diseases

Published: August 29, 2018

A novel p.Pro353His SERPINC1 mutation in the thrombin-binding region affecting stability of Antithrombin molecule in an extended Omani family.

A novel p.Pro353His SERPINC1 mutation in the thrombin-binding region affecting stability of Antithrombin molecule in an extended Omani family.

Journal: International journal of laboratory hematology

Published: March 27, 2018

Haemoglobin Fontainebleau (HBA2: c. 64G>C) in Oman: molecular and haematological characteristics and interaction with various haemoglobinopathies.

Haemoglobin Fontainebleau (HBA2: c. 64G>C) in Oman: molecular and haematological characteristics and interaction with various haemoglobinopathies.

Journal: Journal of clinical pathology

Published: June 12, 2017

Impact of Mannose-Binding Protein Gene Polymorphisms in Omani Sickle Cell Disease Patients.

Impact of Mannose-Binding Protein Gene Polymorphisms in Omani Sickle Cell Disease Patients.

Journal: Mediterranean journal of hematology and infectious diseases

Published: October 09, 2015

Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and β(s) Haplotype: First Report on Comparison between Arab-Indian and African β(s) Genes.

Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and β(s) Haplotype: First Report on Comparison between Arab-Indian and African β(s) Genes.

Journal: Mediterranean journal of hematology and infectious diseases

Published: September 09, 2015

Thiamine responsive megaloblastic anemia: the puzzling phenotype.

Thiamine responsive megaloblastic anemia: the puzzling phenotype.

Journal: Pediatric blood & cancer

Published: July 23, 2013

Potential pitfalls in the diagnosis of Hb Handsworth in areas with high prevalence of HbS.

Potential pitfalls in the diagnosis of Hb Handsworth in areas with high prevalence of HbS.

Journal: International journal of laboratory hematology

Published: July 15, 2013

Showing 1-12 of 17

Last Updated: 09/26/2026