Relationship of foetal haemoglobin levels and βs haplotypes in homozygous sickle cell disease-Reference-Cited by-同舟云学术

Relationship of foetal haemoglobin levels and βs haplotypes in homozygous sickle cell disease

Published:2009-04-24 Issue:1 Volume:45 Page:1-4
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:

Author:

Falusi A. G.,Kulozik A. E.

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1990.tb00405.x/fullpdf

Reference24 articles.

1. Geographical survey of βs- Globin Gene Haplotypes: Evidence for an Independent Asian. Origin of the Sickle - Cell Mutation;Kulozik;Am J Hum Genet,1986

2. Alpha thalassaemia in Nigeria: Its interaction with sickle cell disease;Falusi;Eur J Haematol,1978

3. Clinical Diversity of Sickle Cell Anaemia: Genetic and Cellular Modulation of Disease Severity;Steinberg;Am J Haematol,1983

4. Abnormal haemoglobins in the Sudan Savannah of Nigeria I: Prevalance of haemoglobins and relationships between sickle cell trait, malaria and survival;Fleming;Ann Trop Med Parasit,1979

5. Sickle Cell Anaemia in Tropical Africa;Luzzatto;Clin Haematol,1981

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5. Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease;American Journal of Hematology;1997-01