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J S Waye

Showing results (61-70 of 115) with videos related to

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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.
Genomics|July 1, 1988
Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10P Devilee, T Kievits, J S Waye, 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.
Hemoglobin|February 24, 2001
Second report of Hb Toulon [alpha77(EF6)Pro-->His] in a Canadian family of Italian descentJ S Waye, B Eng, D H Chui, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Treatment of two infants with Cooley's anemia with sodium phenylbutyrateM L MacMillan, M Fouladi, E Nisbet-Brown, et al.
Biotechniques|September 1, 1989
A simple and sensitive method for quantifying human genomic DNA in forensic specimen extractsJ S Waye, L A Presley, B Budowle, 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

Showing results (61-70 of 115) with videos related to

Sort By:
Pageof 12
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.
Genomics|July 1, 1988
Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10P Devilee, T Kievits, J S Waye, 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.
Hemoglobin|February 24, 2001
Second report of Hb Toulon [alpha77(EF6)Pro-->His] in a Canadian family of Italian descentJ S Waye, B Eng, D H Chui, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Treatment of two infants with Cooley's anemia with sodium phenylbutyrateM L MacMillan, M Fouladi, E Nisbet-Brown, et al.
Biotechniques|September 1, 1989
A simple and sensitive method for quantifying human genomic DNA in forensic specimen extractsJ S Waye, L A Presley, B Budowle, 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