An Iranian Child With HbQ-Iran [α75 (EF4) Asp→His]/−α3.7 kb/IVSII.1 G→A

Author:

Rahimi Zohreh,Akramipour Reza,Vaisi-Raygani Asad,Nagel Ronald L.,Muniz Adriana

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference15 articles.

1. Hb D-Punjab [beta 121 (GH4) Glu→Gln]/β0-thalassemia [IVSII.1 (G→A)] in two cases from an Iranian family: First report;Rahimi;Am J Hematol,2006

2. Some notes about HbQ-India and HbQ-Iran;Aksoy;Hemoglobin,1986

3. Two haemoglobins Q, α74 (EF3) and α75 (EF4) Aspartic acid →Histidine;Lorkin;Br J Haematol,1970

4. Human α-thalassemia syndromes: detection of molecular defects;Kattamis;Am J Hematol,1996

5. Hemoglobin Synthesis and Thalassemias. Blood: Principles and Practice of Hematology;Forget,1995

Cited by 4 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. HbD Punjab/HbQ India compound heterozygosity: An unusual association.;Mediterranean Journal of Hematology and Infectious Diseases;2014-11-01

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

3. Hemoglobin Q-Iran detected in family members from Northern Iran: a case report;Journal of Medical Case Reports;2012-02-06

4. Comparative analysis of protein structure of common Hb Q variants;Indian Journal of Pathology and Microbiology;2010

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