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American Journal of Human Genetics|February 1, 1994
Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiersS L Thein, M Sampietro, K Rohde, et al.Human Mutation|January 1, 1994
(ATT) trinucleotide repeats in the antithrombin gene and their use in determining the origin of repeated mutationsR J Olds, D A Lane, V Chowdhury, et al.American Journal of Hematology|June 15, 2007
Sickle liver disease--an unusual presentation in a compound heterozygote for HbS and a novel beta-thalassemia mutationTimothy J S Cross, Philip A Berry, Nuzhat Akbar, et al.Blood|January 1, 1997
Erythroblastic inclusions in dominantly inherited beta thalassemiasP J Ho, S N Wickramasinghe, D C Rees, et al.Blood|February 1, 1988
The polyadenylation site mutation in the alpha-globin gene clusterS L Thein, R B Wallace, L Pressley, et al.Progress in Clinical and Biological Research|January 1, 1987
Raised Hb F levels in sickle cell disease are caused by a determinant linked to the beta globin gene clusterA E Kulozik, S L Thein, B C Kar, et al.Cancer Research|July 1, 1995
Somatic mutations detected by mini- and microsatellite DNA markers reveal clonal intratumor heterogeneity in gastrointestinal cancersS Nagel, B Borisch, S L Thein, et al.British Journal of Haematology|January 1, 1994
Association of a novel high oxygen affinity haemoglobin variant with delta beta thalassaemiaJ Rochette, R Barnetson, L Kiger, et al.Blood|February 1, 1996
Moderate reduction of beta-globin gene transcript by a novel mutation in the 5' untranslated region: a study of its interaction with other genotypes in two familiesP J Ho, J Rochette, C A Fisher, et al.Blood|October 1, 1996
Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiencyD C Rees, J Duley, H A Simmonds, et al.Pageof 15