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Human Genetics|April 1, 1997
Beta-thalassemia and beta[A] globin gene haplotypes in Mexican mestizosA R Villalobos-Arámbula, R Bustos, M Casas-Castañeda, et al.The European Respiratory Journal|June 2, 2006
Computed tomography and pulmonary function abnormalities in sickle cell diseaseK P Sylvester, S R Desai, A U Wells, et al.Lancet (London, England)|August 17, 1985
Feasibility of prenatal diagnosis of beta-thalassaemia with synthetic DNA probes in two Mediterranean populationsS L Thein, J S Wainscoat, J M Old, et al.Hemoglobin|May 1, 1996
Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinopathiesP J Ho, J Rochette, D C Rees, et al.Thrombosis and Haemostasis|August 1, 1994
Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosisV Chowdhury, D A Lane, B Mille, et al.Blood|July 1, 1997
Genetic heterogeneity in heterocellular hereditary persistence of fetal hemoglobinJ E Craig, J Rochette, M Sampietro, et al.British Journal of Haematology|March 1, 1987
Association of thalassaemia intermedia with a beta-globin gene haplotypeS L Thein, J S Wainscoat, M Sampietro, et al.British Journal of Cancer|February 1, 1988
Detection of chromosomal 7 loss in myelodysplasia using an extremely polymorphic DNA probeS L Thein, D G Oscier, A J Jeffreys, et al.Blood|March 1, 1992
Antithrombin III Budapest: a single amino acid substitution (429Pro to Leu) in a region highly conserved in the serpin familyR J Olds, D A Lane, R Caso, et al.Blood|October 27, 1998
Unusually severe heterozygous beta-thalassemia: evidence for an interacting gene affecting globin translationP J Ho, G W Hall, S Watt, et al.Pageof 15