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J S Waye

Showing results (81-90 of 115) with videos related to

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Blood|March 15, 1993
Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemiaW Tang, S P Cai, B Eng, et al.
Thrombosis Research|May 1, 1994
Characterization of a highly polymorphic trinucleotide short tandem repeat within the human antithrombin geneH Ni, J S Waye, R C Austin, et al.
Journal of Medical Genetics|June 19, 2002
Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in CanadaJ S Waye, L M Nakamura, B Eng, et al.
American Journal of Hematology|September 18, 2001
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 casesJ S Waye, B Eng, M Patterson, et al.
Hemoglobin|January 17, 2002
Identification of two new alpha-thalassemia mutations in exon 2 of the alpha1-globin geneJ S Waye, B Eng, M Patterson, et al.
Genomics|September 1, 1987
Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNAJ S Waye, S J Durfy, D Pinkel, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1986
Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage mapsH F Willard, J S Waye, M H Skolnick, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Hemoglobin E/beta thalassemia: the Canadian experienceM Fouladi, M L Macmillan, E Nisbet-Brown, et al.
Blood|March 1, 1991
High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene regionJ S Waye, S P Cai, B Eng, et al.
Clinical Genetics|March 1, 1990
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridizationJ Koch, S Kølvraa, N Hobolt, et al.
Pageof 12

Showing results (81-90 of 115) with videos related to

Sort By:
Pageof 12
Blood|March 15, 1993
Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemiaW Tang, S P Cai, B Eng, et al.
Thrombosis Research|May 1, 1994
Characterization of a highly polymorphic trinucleotide short tandem repeat within the human antithrombin geneH Ni, J S Waye, R C Austin, et al.
Journal of Medical Genetics|June 19, 2002
Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in CanadaJ S Waye, L M Nakamura, B Eng, et al.
American Journal of Hematology|September 18, 2001
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 casesJ S Waye, B Eng, M Patterson, et al.
Hemoglobin|January 17, 2002
Identification of two new alpha-thalassemia mutations in exon 2 of the alpha1-globin geneJ S Waye, B Eng, M Patterson, et al.
Genomics|September 1, 1987
Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNAJ S Waye, S J Durfy, D Pinkel, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1986
Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage mapsH F Willard, J S Waye, M H Skolnick, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Hemoglobin E/beta thalassemia: the Canadian experienceM Fouladi, M L Macmillan, E Nisbet-Brown, et al.
Blood|March 1, 1991
High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene regionJ S Waye, S P Cai, B Eng, et al.
Clinical Genetics|March 1, 1990
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridizationJ Koch, S Kølvraa, N Hobolt, et al.
Pageof 12