New and Known β-Thalassemia Determinants Masked by Known and New δ Gene Defects [Hb A2-Ramallah or δ6(A3)Glu→Gln,GAG>>CAG]-Reference-Cited by-同舟云学术

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New and Known β-Thalassemia Determinants Masked by Known and New δ Gene Defects [Hb A2-Ramallah or δ6(A3)Glu→Gln,GAG>>CAG]

Published:2010-09-20 Issue:5 Volume:34 Page:445-450
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Phylipsen Marion,Harteveld Cornelis L.,Metz Menno de,Gallivan Monica V.E.,Arkesteijn Sandra G.J.,Luo Hong-Yuan,Chui David H.K.,Giordano Piero C.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2010.511591

Reference6 articles.

1. Prospective and retrospective primary prevention of Hemoglobinopathies in multiethnic societies

2. A simple salting out procedure for extracting DNA from human nucleated cells

3. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions

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1. Significance of borderline HbA2 levels in β thalassemia carrier screening;Scientific Reports;2022-03-30

2. An Evaluation for the Causes of Reduced Hb A₂ and the Molecular Characterization of HBD Variants in Hong Kong;Hemoglobin;2021-11-02

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

4. Delta globin gene variations leading to reduction in HbA2levels;International Journal of Laboratory Hematology;2016-07-27

5. HbA2 Measurements in β-Thalassemia and in Other Conditions;Thalassemia Reports;2014-09-29

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