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Journal of Medical Genetics|January 1, 1988
Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindredsS H Sacks, J M Old, S T Reeders, et al.
British Journal of Haematology|November 1, 1982
The interaction of alpha thalassaemia with heterozygous beta thalassaemiaE Kanavakis, J S Wainscoat, W G Wood, et al.
Molecular Biology & Medicine|September 1, 1983
Multiple origins of the sickle mutation: evidence from beta S globin gene cluster polymorphismsJ S Wainscoat, J I Bell, S L Thein, et al.
British Journal of Haematology|March 1, 1995
Thalassaemia in Vanuatu, south-west Pacific: frequency and haematological phenotypes of young childrenM Ganczakowski, D K Bowden, K Maitland, et al.
British Journal of Haematology|June 1, 1985
A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease?J S Wainscoat, S L Thein, D R Higgs, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 31, 1988
Genetic factors as determinants of infectious disease transmission in human communitiesD J Weatherall, J I Bell, J B Clegg, et al.
British Journal of Cancer|April 1, 1987
Detection of somatic changes in human cancer DNA by DNA fingerprint analysisS L Thein, A J Jeffreys, H C Gooi, et al.
British Medical Journal (Clinical Research Ed.)|May 4, 1985
Alpha thalassaemia in British peopleD R Higgs, H Ayyub, J B Clegg, et al.
Journal of Pediatric Hematology/Oncology|December 29, 2000
Iron overload and iron-chelating therapy in hemoglobin E-beta thalassemiaN F Olivieri, S De Silva, A Premawardena, et al.
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