Genetic epidemiology of β-thalassemia in sicily: Do sequences 5′ to theGγ gene and 5′ to the β gene interact to enhance HbF expression in β-thalassemia?-Reference-Cited by-同舟云学术

Genetic epidemiology of β-thalassemia in sicily: Do sequences 5′ to theGγ gene and 5′ to the β gene interact to enhance HbF expression in β-thalassemia?

Published:1992-07 Issue:3 Volume:40 Page:199-206
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Ragusa Angela,Lombardo Mario,Beldjord Cherif,Ruberto Concetta,Lombardo Turi,Elion Jacques,Nagel Ronald L.,Krishnamoorthy Rajagopal

Publisher

Wiley

Subject

Hematology

Reference30 articles.

1. Two independent genetic factors in the beta-globin gene cluster are associated with high G gamma-levels in the HbF of SS patients

2. The -158 site 5' to the G gamma gene and G gamma expression

3. Hematologically and Genetically Distinct Forms of Sickle Cell Anemia in Africa

4. Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.

5. Fetal hemoglobin levels and beta s globin haplotypes in an Indian populations with sickle cell disease

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1. Effect of a group of genetic markers around the 5′ regulatory regions of the β globin gene cluster linked to high HbF on the clinical severity of β thalassemia;Blood Cells, Molecules, and Diseases;2013-03

2. EFFECT OF CIS ACTING POTENTIAL REGULATORS IN THE ß GLOBIN GENE CLUSTER ON THE PRODUCTION OF HBF IN THALASSEMIA PATIENTS;Mediterranean Journal of Hematology and Infectious Diseases;2013-02-16

3. Thalassemia intermedia: An overview;Egyptian Journal of Medical Human Genetics;2012-10

4. Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults;Molecular Biology Reports;2011-09-27

5. Molecular Analysis of β-Thalassemia Patients: First Identification of Mutations HBB:c.93-2A>G and HBB:c.114G>A in Brazil;Hemoglobin;2011-07-28