The Carrier Frequency of α-Globin Gene Triplication in an Iranian Population with Normal or Borderline Hematological Parameters-Reference-Cited by-同舟云学术

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The Carrier Frequency of α-Globin Gene Triplication in an Iranian Population with Normal or Borderline Hematological Parameters

Published:2011-07-28 Issue:4 Volume:35 Page:323-330
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Moosavi Seyedeh Fatemeh,Amirian Azam,Zarbakhsh Behnaz,Kordafshari Alireza,Mirzahoseini Hasan,Zeinali Sirous,Karimipoor Morteza

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2011.571527

Reference24 articles.

1. Iranian national thalassaemia screening programme

2. Molecular spectrum of ?-thalassemia in the Iranian population of Hormozgan: Three novel point mutation defects

3. 4 Pathophysiology of thalassaemia

4. Phenotype—genotype relationships in monogenic disease: lessons from the thalassaemias

5. The triplicated α-globin gene locus in β-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies

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1. Development and clinical validation of a novel detection kit for α-thalassemia in southern Chinese;Frontiers in Genetics;2024-09-05

2. Epidemiological Survey of Hemoglobinopathies Based on Next-Generation Sequencing Platform in Hunan Province, China*;BIOMED ENVIRON SCI;2023

3. Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual;eJHaem;2021-07-19

4. RETROSPECTIVE ANALYSIS OF ALPHA GLOBIN COPY NUMBER VARIATIONS DETERMINED BY MLPA IN THE TRAKYA REGION;İstanbul Tıp Fakültesi Dergisi;2021-07-02

5. Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers;Mutation Research/Reviews in Mutation Research;2021-07

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