Molecular Characterization of Homozygous (High HbA2) β-Thalassemia Intermedia in Greece-Reference-Cited by-同舟云学术

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

Published:1995-01 Issue:1 Volume:12 Page:37-45
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Kanavakis Emmanuel,Traeger-Synodinos Joanne,Tzetis Maria,Metaxotou-Mavromati Anna,Ladis Vasilis,Kattamis Christos

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.3109/08880019509029526

Reference23 articles.

1. FREQUENCIES OF COMMON β-THALASSAEMIA ALLELES AMONG DIFFERENT POPULATIONS: VARIABILITY IN CLINICAL SEVERITY

2. Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations

3. Genetic and Molecular Analysis of Mild Forms of Homozygous ?-Thalassemia

4. Thalassaemia intermedia in Cyprus: the interaction of α and β thalassaemia

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1. Molecular Basis of β-Thalassemia Intermedia in Erbil Province of Iraqi Kurdistan;Hemoglobin;2015-04-22

2. Congestive Heart Failure and Treatment in Thalassemia Major;Hemoglobin;2008-01

3. Molecular Basis of Thalassemia Intermedia in Iran;Hemoglobin;2008-01

4. Thalassemia intermedia today: should patients regularly receive transfusions?;Transfusion;2007-05

5. Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia;European Journal of Haematology;2006-04

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