Gγ −37 (A→T): A New Nondeletional Hereditary Persistence of Fetal Hemoglobin Determinant Associated with the Rare Codon 91 (+T) δ0-Thalassemia-Reference-Cited by-同舟云学术

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Gγ −37 (A→T): A New Nondeletional Hereditary Persistence of Fetal Hemoglobin Determinant Associated with the Rare Codon 91 (+T) δ0-Thalassemia

Published:2006-01 Issue:3 Volume:30 Page:371-377
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Bouva Marelle J.,Harteveld Cornelis L.,Bakker-Verweij Greet,van Delft Peter,Giordano Piero C.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260600755641

Reference8 articles.

1. 7 Increased HbF in adult life

2. A novel ?� arising from a frameshift insertion, detected by direct sequencing of enzymatically amplified DNA

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

4. Analysis of ?-globin gene haplotypes in Asian Indians: origin and spread of ?-thalassaemia on the Indian subcontinent

Cited by 5 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. The relationship between the variations in GÎ³ and AÎ³ promotors and the Hereditary Persistence of Fetal Hemoglobin (HPFH);Cellular and Molecular Biology;2018-01-31

2. Alterations on high HbF levels may be associated with KLF1 gene mutations;Cellular and Molecular Biology;2017-08-30

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

4. Occurrence of common and rare δ-globin gene defects in two multiethnic populations: thirteen new mutations and the significance of δ-globin gene defects in β-thalassemia diagnostics;International Journal of Laboratory Hematology;2010-07-29

5. The relevance of hemoglobin F measurement in the diagnosis of thalassemias and related hemoglobinopathies;Clinical Biochemistry;2009-12

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