Ocular findings in Saudi Arabian patients with sickle cell disease.

Author:

al-Hazzaa S,Bird A C,Kulozik A,Serjeant B E,Serjeant G R,Thomas P,Padmos A

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference7 articles.

1. Two different forms of homozygous sickle cell disease occur in Saudi Arabia;Padmos, M.A.; Roberts, G.T.; Sackey, K.; Kulozik, A.; Bail, S.; Morris, J.S.,1991

2. Geographical survey of, B-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation;Kulozik, A.E.; Wainscoat, J.S.; Serjeant, G.R.; Kar, B.C.; Al-Awamy, B.; Essan, G.J.F.;Am 7 Hum Genet,1986

3. Fetal haemoglobin production and the sickle gene in the Oases of Eastern Saudi Arabia;Pembrey, M.E.; Wood, W.G.; Weatherall, D.J.; Perrine, R.P.;BrJ Haematol,1978

4. Sickle cell disease;Serjeant, G.R.,1992

5. A new classification of peripheral retinal vascular changes in sickle cell disease: relevance to sight threatening disease;Penman, A.D.; Talbot, J.F.; Chuang, E.L.; Thomas, P.; Serjeant, G.R.; Bird, A.C.,1994

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