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Human Mutation|January 1, 1994
Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencingR D Hain, D Chitayat, R Cooper, et al.Blood|March 1, 1992
Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin geneS P Cai, B Eng, W H Francombe, et al.American Journal of Hematology|October 1, 1991
Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotypeJ S Waye, D H Chui, B Eng, et al.American Journal of Hematology|September 1, 1995
Severity of beta-thalassemia due to genotypes involving the IVS-I-6 (T-->C) mutationJ S Waye, B Eng, M Patterson, et al.American Journal of Hematology|December 1, 1994
Hb E/Hb LeporeHollandia in a family from BangladeshJ S Waye, B Eng, M Patterson, et al.British Journal of Haematology|November 28, 2001
Hb H hydrops foetalis syndrome: a case report and review of literatureF Lorey, P Charoenkwan, H E Witkowska, et al.Chromosoma|October 1, 1989
Concerted evolution of alpha satellite DNA: evidence for species specificity and a general lack of sequence conservation among alphoid sequences of higher primatesJ S Waye, H F WillardApplied and Theoretical Electrophoresis : the Official Journal of the International Electrophoresis Society|January 1, 1990
Agarose gel electrophoresis of linear genomic DNA in the presence of ethidium bromide: band shifting and implications for forensic identity testingJ S Waye, R M FourneyJournal of Molecular Evolution|January 1, 1987
Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeatH F Willard, J S WayeMolecular and Cellular Biology|September 1, 1986
Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosomeJ S Waye, H F WillardPageof 23