Molecular Basis of β-Thalassemia Intermedia in Erbil Province of Iraqi Kurdistan-Reference-Cited by-同舟云学术

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Molecular Basis of β-Thalassemia Intermedia in Erbil Province of Iraqi Kurdistan

Published:2015-04-22 Issue:3 Volume:39 Page:178-183
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Shamoon Rawand P.,Al-Allawi Nasir A. S.,Cappellini Maria D.,Di Pierro Elena,Brancaleoni Valentina,Granata Francesca

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1032415

Reference32 articles.

1. The Thalassaemia Syndromes

2. Molecular Characterization of Homozygous (High HbA2) β-Thalassemia Intermedia in Greece

3. Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

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1. Hb SKMC and an unprecedented γδβ-thalassemia: first report from Iraq;Hematology;2024-09-09

2. Unveiling the molecular and comorbidity profile among transfusion-dependent and nontransfusion-dependent beta-thalassemic patients in Baghdad city;Iraqi Journal of Hematology;2024-08-19

3. Magnitude of Bone Disease in Transfusion-Dependent and Non-Transfusion-Dependent β-Thalassemia Patients;Cureus;2024-03-12

4. A Population-Oriented Genetic Scoring System to Predict Phenotype: A Pathway to Personalized Medicine in Iraqis With β-Thalassemia;Hemoglobin;2024-02-23

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