Some notes about HB Q-India and HB Q-Iran-Reference-Cited by-同舟云学术

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Some notes about HB Q-India and HB Q-Iran

Published:1986-01 Issue:2 Volume:10 Page:215-219
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Aksoy M.,Gurgey A.,Altay C.,Kilinc Y.,Carstairs K. C.,Kutlar A.,Chen S. S.,Webber B. B.,Wilson J. B.,Huisman T. H. J.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630268609046447

Reference12 articles.

1. Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families.

2. Hemoglobin QIndia, α64(E l3) Asp→His, and β- Thalassemiaina Canadian Family

3. Hemoglobin G Taichung: α74 Asp → His

4. Hemoglobin Mahidol: a new hemoglobin α-chain mutant

5. The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG- alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia

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 prevalence and genotypes of alpha-thalassemia in Adıyaman: two rare alpha variants;Turkish Journal of Biochemistry;2016-01-01

2. Genetic Epidemiology, Hematological and Clinical Features of Hemoglobinopathies in Iran;BioMed Research International;2013

3. A New Hemoglobin Variant: Hb Izmir [β86(F2)Ala→Val, GCC>GTC; HBB:c.260C>T];Hemoglobin;2012-06

4. The first use of EaeI restriction enzyme in DNA diagnosis of Hb Q-India;International Journal of Laboratory Hematology;2011-03

5. An Iranian Child With HbQ-Iran [α75 (EF4) Asp→His]/−α3.7 kb/IVSII.1 G→A;Journal of Pediatric Hematology/Oncology;2007-09

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