Gall stones in Jamaican children with homozygous sickle cell disease.

Author:

Webb D K,Darby J S,Dunn D T,Terry S I,Serjeant G R

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference20 articles.

1. Screening cord bloods for detection of sickle cell disease;t Serjeant BE; M, Forbes; LL, Williams; GR, Serjeant;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.;Br J Haematol,1981

3. Haemoglobin gene frequencies in the Jamaican population: a study in 100,000 newborns;Serjeant, G.R.; Serjeant, B.E.; Forbes, M.; Hayes, R.J.; Higgs, D.R.; Lehmann, H.;Br J Haematol,1986

4. Chi-square tests with one degree of freedom; extensions of the Mantel-Haenszel procedure;Mantel, N.;Journal of American Statistical Association,1963

5. The prevalence of cholelithiasis in sickle cell disease as diagnosed by ultrasound and cholecystography;s LachmanBS; J, Lazerson; RJ, Starshak; FM, Vaughters; SL, Werlin;Pediatrics,1979

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