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Hemoglobin|January 1, 1995
Identification of a new high oxygen affinity hemoglobin variant: Hb Aurora [beta 139(H17) Asn-->Tyr]J Lafferty, M Ali, K Matthew, et al.American Journal of Hematology|November 26, 1997
De novo mutation of the beta-globin gene initiation codon (ATG-->AAG) in a Northern European boyJ S Waye, B Eng, M Patterson, et al.American Journal of Hematology|June 1, 1994
Genetic linkage studies in antithrombin-deficient kindreds using a highly polymorphic trinucleotide short tandem repeat (STR) within the human antithrombin geneH Ni, J S Waye, W P Sheffield, et al.American Journal of Medical Genetics|April 12, 2001
DHCR7 genotypes of cousins with Smith-Lemli-Opitz syndromeM J Nowaczyk, T Heshka, B Eng, et al.Molecular and Cellular Probes|April 1, 1994
Trinucleotide repeat polymorphism within the human antithrombin gene (AT3): allele frequency data for three population groupsJ S Waye, B Eng, H Y Ni, et al.Human Mutation|January 1, 1993
Identification of two novel beta zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a beta-globin gene deletionB Eng, D H Chui, J Saunderson, et al.Lancet (London, England)|November 6, 1993
Immunocytological test to detect adult carriers of (--SEA/) deletional alpha-thalassaemiaW Tang, H Y Luo, B Eng, et al.American Journal of Hematology|December 1, 1992
Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin KenyaJ S Waye, S P Cai, B Eng, et al.American Journal of Physical Anthropology|May 19, 1998
Technical note: improved DNA extraction from ancient bones using silica-based spin columnsD Y Yang, B Eng, J S Waye, et al.American Journal of Medical Genetics|August 15, 2001
Frequency and ethnic distribution of the common DHCR7 mutation in Smith-Lemli-Opitz syndromeM J Nowaczyk, L M Nakamura, B Eng, et al.Pageof 12