Hb H Disease Among Tunisians: Molecular Characterization of α‐Thalassemia Determinants and Hematological Findings-Reference-Cited by-同舟云学术

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Hb H Disease Among Tunisians: Molecular Characterization of α‐Thalassemia Determinants and Hematological Findings

Published:2003-01 Issue:1 Volume:27 Page:57-61
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Zorai Amine,Abbes Salem,Préhu Claude,Omar Souheil,Gerard Nathalie,Hafsia Raouf,Asma Bouaziz,Guemira Fethi,Dellagi Kousay

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1081/HEM-120018439

Reference19 articles.

1. α Thalassemia

2. A review of the molecular genetics of the human alpha-globin gene cluster

3. α-Thalassaemia as a result of a novel splice donor site mutation of the α1 -globin gene

4. α-Thalassaemia caused by a polyadenylation signal mutation

5. Mutation in an intervening sequence splice junction in man.

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region;Hemoglobin;2020-01-02

2. Rare hemoglobin variants in Tunisian population;International Journal of Laboratory Hematology;2014-06-06

3. Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience;Hemoglobin;2014-05-14

4. Identification of four common α-thalassemia gene deletions among a group with hemoglobinopathies in Sétif population, Algeria;pteridines;2013-11-19

5. α-Thalassemia Frequency and Mutations in Children with Hypochromic Microcytic Anemias and Relation with β-Thalassemia, Iron Deficiency Anemia;Pediatric Hematology and Oncology;2012-03-30

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