Frequencies and phenotypic consequences of association of α- and β-thalassemia alleles with sickle-cell disease in Bahrain-Reference-Cited by-同舟云学术

Frequencies and phenotypic consequences of association of α- and β-thalassemia alleles with sickle-cell disease in Bahrain

Published:2016-12-16 Issue:1 Volume:39 Page:76-83
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int. Jnl. Lab. Hem.

Author:

Abuamer S.¹,Shome D. K.¹,Jaradat A.²,Radhi A.³,Bapat J. P.³,Sharif K. A.⁴,Al-Touq J.⁴,Al-Asheeri A.⁴,Al-Ajami A.⁴

Affiliation:

1. Department of Pathology and Al Jawhara Centre for Molecular Medicine and Inherited Disorders; College of Medicine and Medical Sciences; Arabian Gulf University; Manama Kingdom of Bahrain

2. Department of Family and Community Medicine; College of Medicine and Medical Sciences; Arabian Gulf University; Manama Kingdom of Bahrain

3. Department of Pathology; Salmaniya Medical Complex; Manama Kingdom of Bahrain

4. Department of Internal Medicine; Salmaniya Medical Complex; Manama Kingdom of Bahrain

Funder

Arabian Gulf University College of Medicine and Medical Sciences, Research and Ethics Committee

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijlh.12577/fullpdf

Reference40 articles.

1. Clinical diversity of sickle cell anemia: genetic and cellular modulation of disease severity;Steinberg;Am J Hematol,1983

2. Sickle cell anemia as a syndrome: a review of diagnostic features;Huisman;Am J Hematol,1979

3. Effect of alpha thalassaemia on the rheology of homozygous sickle cell disease;Serjeant;Br J Haematol,1983

4. Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia;Steinberg;Blood,1984

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