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

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General Info

Geography

Oman (OMN)

United Arab Emirates (ARE)

Yemen (YEM)

Time period covered

01/1985 - 12/1985

Data type

Scientific literature

Keywords

G6PD deficiency, Sickle cell disorders, Thalassemias

Citation

Authors

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

Journal

J Med Genet

Volume

Issue

Pages

245-51

Publication year

1986

Suggested citation

White JM, Byrne M, Richards R, Buchanan T, Katsoulis E, Weerasingh K. Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia. J Med Genet. 1986; 23(3): 245-51.

GHDx Entry last modified on: May 21, 2023

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

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