Sickle cell retinopathy in Jamaican children: further observations from a cohort study.

Author:

Talbot J F,Bird A C,Maude G H,Acheson R W,Moriarty B J,Serjeant G R

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference17 articles.

1. Screening cord bloods for detection of sickle cell disease;Serjeant, B.E.; Forbes, M.; Williams, L.L.;in Jamaica. Clin Chem,1974

2. The development of haematological changes in homozygous sickle cell disease: a cohort study from birth to 6 years;Serjeant, G.R.; Grandison, Y.; Lowrie, Y.; etal;Br J Haematol,1981

3. Estimation of small percentages of foetal haemoglobin;Betke, K.; Marti, H.R.; Schlicht, I.;Nature,1959

4. The interaction of alphathalassemia and homozygous sickle-cell disease;Higgs, D.R.; Aldridge, B.E.; Lamb, J.;N Engl J Med,1982

5. Dark-without-pressure fundus lesions;Nagpal, K.C.; Goldberg, M.F.; Asdourian, G.; Goldbaum, M.; Huamonte, F.;Br J Ophthalmol,1975

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