The association of Hb khartoum [β124(H2)Pro→Arg] with γ+-thalassemia is responsible for hemolytic disease in the newborn of a sudanese family-Reference-Cited by-同舟云学术

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The association of Hb khartoum [β124(H2)Pro→Arg] with γ+-thalassemia is responsible for hemolytic disease in the newborn of a sudanese family

Published:1999-01 Issue:1 Volume:23 Page:33-45
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Bayoumi R. A.,Dawodu A.,Qureshi M. M.,Al-Khider A.,Fitzgerald P.,Riou J.,Fisher C. A.,Fitches A.,Old J. M.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269908996146

Reference13 articles.

1. Two New Haemoglobin Variants involving Proline Substitutions

2. Hemoglobin Philly (β35 tyrosine→phenylalanine): studies in the molecular pathology of hemoglobin

3. Structural characterization of hemoglobin Tacoma

4. VARIATIONS IN THE STRUCTURE OF HUMAN HAEMOGLOBIN

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1. Hb F-Zhejiang: A Hb F Variant Due to A NovelGγ Mutation [Gγ101(G3)Glu→Gln,GAG>CAG] Detected in a Chinese Newborn;Hemoglobin;2010-01

2. Genetic Disorders in Sudan;Genetic Disorders Among Arab Populations;2010

3. Two NewGγ Chain Variants: Hb F-Saint-Etienne [Gγ79(EF3)Asp→His] and Hb F-Lyon [Gγ97(FG4)His→Arg];Hemoglobin;2008-01

4. A NewGγ Chain Variant: Hb F-Bron [γ20(B2)Val→Ala];Hemoglobin;2005-01

5. The molecular basis for the thalassaemias in Sri Lanka;British Journal of Haematology;2003-05

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