original ) (raw )A Novel Mutation in the α2-Globin Gene in Two Unrelated Iranian Families
Hosein Azimian
Shiraz E-Medical Journal, 2014
View PDFchevron_right
First report of the spectrum of δ-globin gene mutations in Omani subjects - identification of novel mutations
Salam Alkindi
International Journal of Laboratory Hematology, 2014
View PDFchevron_right
Coinheritance of the c.-19 G > C and c.315 + 1 G > A Variants in the β-Globin Gene Leads to Thalassemia Disease: A Report from the North of Iran
mahan mahdavi
Case Reports in Genetics
View PDFchevron_right
Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family
mohammad Taghi Akbari
Annals of Hematology, 2010
View PDFchevron_right
β-Globin Mutations in Egyptian Patients With β-Thalassemia
Ebtesam Abdalla
Laboratory medicine, 2015
View PDFchevron_right
α-thalassaemia masked by β gene defects and a new polyadenylation site mutation on the α2-globin gene
Wytze Oosterhuis
European Journal of Haematology, 2010
View PDFchevron_right
A 21 Nucleotide Duplication on the α 1- and α 2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease
Samaneh Farashi
Hemoglobin, 2015
View PDFchevron_right
Molecular Basis of Beta Thalassemia Mutations in Egyptian Patients
ahmed daif
Research Journal of Applied Biotechnology, 2017
View PDFchevron_right
A Novel Alpha-thalassemia Nonsense Mutation in HBA2: C.382 A > T globin Gene
Ahmad Ahmadzadeh
Archives of Iranian Medicine, 2014
View PDFchevron_right
Incidence of Alpha-Globin Gene Defect in the Lebanese Population: A Pilot Study
Farah Fares
BioMed Research International, 2015
View PDFchevron_right
Identification of Two Rare β-Globin Gene Mutations in a Patient with β-Thalassemia Intermedia from Azerbaijan
Chingiz Asadov
Hemoglobin, 2013
View PDFchevron_right
A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran
ali banihashemi
Hemoglobin, 2017
View PDFchevron_right
Molecular spectrum of α-globin gene mutations in the Aegean region of Turkey: first observation of three α-globin gene mutations in the Turkish population
Yesim Aydinok
International Journal of Hematology, 2015
View PDFchevron_right
Molecular Basis of α-Thalassemia in Iran
Atefeh Valaei
Iranian Biomedical Journal, 2018
View PDFchevron_right
Molecular characterization of β-globin gene mutations in Malay patients with Hb E-β-thalassaemia and thalassaemia major
edwin putra
1989
View PDFchevron_right
The First Report of a 290-bp Deletion in β-Globin Gene in the South of Iran
Mohammad Hamid
Iranian biomedical journal, 2016
View PDFchevron_right
A Novel Alpha-thalassemia Nonsense Mutation in HBA2:C.382 A > T globin GeneMoham
Mohammad Ali Hamid
View PDFchevron_right
Scanning of ?-globin gene for identification of ?-thalassemia mutation in Romanian population
Daniel Coriu
Journal of Cellular and Molecular Medicine, 2004
View PDFchevron_right
Molecular characterization of β-globin gene mutations in patients with β-thalassaemia intermedia in South China
Stylianos Antonarakis
British Journal of Haematology, 1988
View PDFchevron_right
Screening of Iranian Thalassemic Families for the Most Common Deletions of the β-Globin Gene Cluster
Navid Almadani
Hemoglobin, 2007
View PDFchevron_right
A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family AcquiredDe Novo
Abu Sufian
Hemoglobin, 2019
View PDFchevron_right
Molecular patterns of alpha-thalassemia in the kingdom of Saudi Arabia: identification of prevalent genotypes and regions with high incidence
Heba Elmasry
Thrombosis Journal
View PDFchevron_right
Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia
Hossam Murad
BMC Pediatrics
View PDFchevron_right
Co-Inheritance of Beta & Delta-Globin Gene (HbYialousa) Mutations in an Iranian β -Thalassemia Carrier
Farnaz Eghbalpour
International Journal of Clinical Medicine, 2012
View PDFchevron_right
Spectrum of Beta Globin Gene Mutations in Egyptian Children with Β- Thalassemia
M. Hamdy
Mediterranean Journal of Hematology and Infectious Diseases, 2014
View PDFchevron_right
Molecular Spectrum of α -Globin Gene Defects in the Omani Population
Piero Giordano
Hemoglobin, 2014
View PDFchevron_right
Molecular basis of alpha-thalassemia in Algeria
Jacques Elion
Hemoglobin, 2008
View PDFchevron_right
Alpha thalassemia gene mutations in neonates from Mazandaran, Iran, 2012
Hossein Jalali
Hematology, 2013
View PDFchevron_right
Known and New δ-Globin Gene Mutations and Other Factors Influencing Hb A 2 Measurement in the Omani Population
Piero Giordano
Hemoglobin, 2014
View PDFchevron_right
Spectrum of β thalassemia mutations and HbF levels in the heterozygous Moroccan population
Mohamed Khatab
American Journal of Hematology, 2003
View PDFchevron_right
Co-inheritance of --MED double gene deletion and αααAnti3.7 triplication on α-globin gene in Mazandaran at 2016
Hossein Jalali
Research in Molecular Medicine, 2017
View PDFchevron_right
Alpha thalassaemia due to non-deletional mutations on the -3.7 alpha globin fusion gene
Reza Ghassemifar
Pathology, 2013
View PDFchevron_right
Hb Narges Lab, a Novel Hemoglobin Variant of the β-Globin Gene
Alihossein Saberi
Archives of Iranian Medicine
View PDFchevron_right
Alpha globine gene mutations in a case series of Kurdish Iranian alpha thalassemia patients
Mohammad-sadegh Fallah
Scientific journal of Kurdistan University of Medical Sciences, 2015
View PDFchevron_right
Mutational Studies of Gene HBB in β-Thalassemia Patients from Balochistan, Pakistan
Muneeza Arbab
Current Trends in OMICS, 2021
View PDFchevron_right