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N T Bech-Hansen

Showing results (21-30 of 51) with videos related to

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Nucleic Acids Research|May 25, 1989
TaqI RFLP in human adenylate kinase-1 (AK1) gene region on chromosome 9N T Bech-Hansen, K J Marshall, S L Kraus
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1983
Restriction fragment length polymorphisms associated with immunoglobulin C gamma genes reveal linkage disequilibrium and genomic organizationN T Bech-Hansen, P S Linsley, D W Cox
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|July 20, 2000
Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1FK M Boycott, W G Pearce, N T Bech-Hansen
Genomics|June 30, 2000
Isolation and characterization of a calcium channel gene, Cacna1f, the murine orthologue of the gene for incomplete X-linked congenital stationary night blindnessM J Naylor, D E Rancourt, N T Bech-Hansen
Journal of the National Cancer Institute|July 1, 1977
Rapid assays for evaluating the drug sensitivity of tumor cellsN T Bech-Hansen, F Sarangi, D J Sutherland, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1983
Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locusP S Linsley, N T Bech-Hansen, L Siminovitch, et al.
Genomics|May 1, 1996
A 2-megabase physical contig incorporating 43 DNA markers on the human X chromosome at p11.23-p11.22 from ZNF21 to DXS255K M Boycott, G R Halley, D Schlessinger, et al.
Radiation Research|May 1, 1982
Impaired colony-forming ability following gamma irradiation of skin fibroblasts from tuberous sclerosis patientsM C Paterson, B M Sell, B P Smith, et al.
Cancer Research|June 1, 1981
Association of in vitro radiosensitivity and cancer in a family with acute myelogenous leukemiaN T Bech-Hansen, B M Sell, J J Mulvihill, et al.
Gene|February 5, 1999
Physical map covering a 2 Mb region in human xp11.3 distal to DX6849K L Stoddart, C Jermak, R Nagaraja, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Nucleic Acids Research|May 25, 1989
TaqI RFLP in human adenylate kinase-1 (AK1) gene region on chromosome 9N T Bech-Hansen, K J Marshall, S L Kraus
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1983
Restriction fragment length polymorphisms associated with immunoglobulin C gamma genes reveal linkage disequilibrium and genomic organizationN T Bech-Hansen, P S Linsley, D W Cox
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|July 20, 2000
Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1FK M Boycott, W G Pearce, N T Bech-Hansen
Genomics|June 30, 2000
Isolation and characterization of a calcium channel gene, Cacna1f, the murine orthologue of the gene for incomplete X-linked congenital stationary night blindnessM J Naylor, D E Rancourt, N T Bech-Hansen
Journal of the National Cancer Institute|July 1, 1977
Rapid assays for evaluating the drug sensitivity of tumor cellsN T Bech-Hansen, F Sarangi, D J Sutherland, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1983
Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locusP S Linsley, N T Bech-Hansen, L Siminovitch, et al.
Genomics|May 1, 1996
A 2-megabase physical contig incorporating 43 DNA markers on the human X chromosome at p11.23-p11.22 from ZNF21 to DXS255K M Boycott, G R Halley, D Schlessinger, et al.
Radiation Research|May 1, 1982
Impaired colony-forming ability following gamma irradiation of skin fibroblasts from tuberous sclerosis patientsM C Paterson, B M Sell, B P Smith, et al.
Cancer Research|June 1, 1981
Association of in vitro radiosensitivity and cancer in a family with acute myelogenous leukemiaN T Bech-Hansen, B M Sell, J J Mulvihill, et al.
Gene|February 5, 1999
Physical map covering a 2 Mb region in human xp11.3 distal to DX6849K L Stoddart, C Jermak, R Nagaraja, et al.
Pageof 6