Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia.-Reference-Cited by-同舟云学术

Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia.

Published:1986-06-01 Issue:3 Volume:23 Page:245-251
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

White J M,Byrne M,Richards R,Buchanan T,Katsoulis E,Weerasingh K

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference11 articles.

1. Blood groups and types, hemoglobin variants, and G-6-PD deficiency among Abu Dhabians in the United Arab Emirates;Kamel, K.; Chandy, R.; Mousa, H.; Yunis, D.;Am J Phys Anthropol

2. Differentiation of iron deficiency from thalassaemia trait by routine blood count;England, J.M.; Frazer, P.M.;Lancet,1973

3. An evaluation of the methods for quantitation of hemoglobin A2. Results from a survey of 10,063 cases;Efremov, G.D.;Hemoglobin,1977

4. Thalassaemia genes in Peninsular Arabs;White, J.M.; Richards, R.; Buchanan, T.;Br J Haematol,1985

5. Abnormal haemoglobins;White, J.M.; Frost, B.,1984

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