Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype-Reference-Cited by-同舟云学术

Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype

Published:2013-06 Issue:1 Volume:51 Page:22-26
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Ngo Duyen,Bae Harold,Steinberg Martin H.,Sebastiani Paola,Solovieff Nadia,Baldwin Clinton T.,Melista Efthymia,Safaya Surinder,Farrer Lindsay A.,Al-Suliman Ahmed M.,Albuali Waleed H.,Al Bagshi Muneer H.,Naserullah Zaki,Akinsheye Idowu,Gallagher Patrick,Luo Hong-yuan,Chui David H.K.,Farrell John J.,Al-Ali Amein K.,Alsultan Abdulrahman

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference42 articles.

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2. Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation;Galarneau;Nat. Genet.,2010

3. Individual variation in the production and survival of F cells in sickle-cell disease;Dover;N. Engl. J. Med.,1978

4. DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease;Lettre;Proc. Natl. Acad. Sci. U. S. A.,2008

5. Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans;Bae;Blood,2012

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