Associated Papers
Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies.
Tamana S et al.
Elife, 2022
Clinical and genetic characteristics of hemoglobin H disease in Iran.
Abolghasemi H et al.
Pediatric Hematology and Oncology, 2022
α-Thalassemia Mutations in Ilam Province, West Iran.
Moradi K et al.
Hemoglobin, 2022
A Novel β0-Thalassemia Mutation, HBB: c.356_357delTT [Codon 118 (-TT)] in an Iraqi Kurd.
Atroshi SD et al.
Hemoglobin, 2021
Molecular Genetic Analysis of α-Thalassemia in Hamadan Province, West Iran.
Moradi K et al.
Hemoglobin, 2020
The Spectrum of α-Thalassemia Mutations in Kurdistan Province, West Iran.
Alibakhshi R et al.
Hemoglobin, 2020
α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region.
Al-Riyami AZ et al.
Hemoglobin, 2020
Iranian patients with hemoglobin H disease: genotype-phenotype correlation.
Paridar M et al.
Molecular Biology Reports, 2019
Characterization of deletional and non-deletional alpha globin variants in a large cohort from Spain between 2009 and 2014.
de la Fuente-Gonzalo F et al.
Annals of Hematology, 2019
The Spectrum of α-Thalassemia Mutations in the Lak Population of Iran.
Moradi K et al.
Hemoglobin, 2019
A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran.
Eftekhari H et al.
Hemoglobin, 2017
Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran.
Derakhshan SM et al.
Hemoglobin, 2016
Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran.
Miri-Moghaddam E et al.
Hemoglobin, 2016
Point mutations which should not be overlooked in Hb H disease.
Farashi S et al.
Expert Review of Hematology, 2016
Evaluation of α-Globin Gene Mutations Among Different Ethnic Groups in Khuzestan Province, Southwest Iran.
Khosravi A et al.
Hemoglobin, 2016
Diagnostic pitfalls of less well recognized HbH disease.
Farashi S et al.
Blood Cells, Molecules & Diseases, 2015
The Spectrum of α-Thalassemia Mutations in Kermanshah Province, West Iran.
Alibakhshi R et al.
Hemoglobin, 2015
Molecular spectrum of α-globin gene defects in the Omani population.
Hassan SM et al.
Hemoglobin, 2014
The spectrum of α-thalassemia mutations in the Kurdish population of Northeastern Iraq.
Al-Allawi NA et al.
Hemoglobin, 2013
Novel mutations responsible for α-thalassemia in Iranian families.
Bayat N et al.
Hemoglobin, 2013
Sickle cell disease in the Kurdish population of northern Iraq.
Al-Allawi NA et al.
Hemoglobin, 2012
Genotype-phenotype correlation in Iranian patients with Hb H disease.
Ebrahimkhani S et al.
Hemoglobin, 2011
Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE).
Al-Gazali L et al.
Human Mutation, 2010