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N T Bech-Hansen

Showing results (31-40 of 51) with videos related to

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Brain Research|June 1, 1988
Selective messenger RNA reduction in Alzheimer's diseaseD R McLachlan, W J Lukiw, L Wong, et al.
Genomics|August 22, 2000
Development of a 1.4-Mb BAC/PAC contig and physical map within the critical region for complete X-linked congenital stationary night blindness in Xp11.4R L Sparkes, C G Summer, K M Boycott, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 1, 1997
The phakomatoses: recent advances in geneticsI M MacDonald, N T Bech-Hansen, W A Britton, et al.
Journal of Medical Genetics|March 1, 2006
X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F geneR Jalkanen, M Mäntyjärvi, R Tobias, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Integration of 101 DNA markers across human Xp11 using a panel of somatic cell hybridsK M Boycott, B J Moore, K J Gratton, et al.
Genomics|May 1, 1994
Clustered organization of Krüppel zinc-finger genes at Xp11.23, flanking a translocation breakpoint at OATL1: a physical map with locus assignments for ZNF21, ZNF41, ZNF81, and ELK1J C Knight, G Grimaldi, H J Thiesen, et al.
Cancer Investigation|January 1, 1983
Radiogenic male breast cancer with in vitro sensitivity to ionizing radiation and bleomycinM H Greene, J J Goedert, N T Bech-Hansen, et al.
Human Genetics|October 6, 1998
Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23N T Bech-Hansen, K M Boycott, K J Gratton, et al.
The American Journal of Medicine|February 1, 1983
Acute leukemia after radiotherapy in a patient with Turcot's syndrome. Impaired colony formation in skin fibroblast cultures after irradiationF P Li, J B Little, N T Bech-Hansen, et al.
Genomics|April 18, 1998
Construction of a 1.5-Mb bacterial artificial chromosome contig in Xp11.23, a region of high gene contentK M Boycott, R J Zahorchak, C G Summer, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Brain Research|June 1, 1988
Selective messenger RNA reduction in Alzheimer's diseaseD R McLachlan, W J Lukiw, L Wong, et al.
Genomics|August 22, 2000
Development of a 1.4-Mb BAC/PAC contig and physical map within the critical region for complete X-linked congenital stationary night blindness in Xp11.4R L Sparkes, C G Summer, K M Boycott, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 1, 1997
The phakomatoses: recent advances in geneticsI M MacDonald, N T Bech-Hansen, W A Britton, et al.
Journal of Medical Genetics|March 1, 2006
X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F geneR Jalkanen, M Mäntyjärvi, R Tobias, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Integration of 101 DNA markers across human Xp11 using a panel of somatic cell hybridsK M Boycott, B J Moore, K J Gratton, et al.
Genomics|May 1, 1994
Clustered organization of Krüppel zinc-finger genes at Xp11.23, flanking a translocation breakpoint at OATL1: a physical map with locus assignments for ZNF21, ZNF41, ZNF81, and ELK1J C Knight, G Grimaldi, H J Thiesen, et al.
Cancer Investigation|January 1, 1983
Radiogenic male breast cancer with in vitro sensitivity to ionizing radiation and bleomycinM H Greene, J J Goedert, N T Bech-Hansen, et al.
Human Genetics|October 6, 1998
Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23N T Bech-Hansen, K M Boycott, K J Gratton, et al.
The American Journal of Medicine|February 1, 1983
Acute leukemia after radiotherapy in a patient with Turcot's syndrome. Impaired colony formation in skin fibroblast cultures after irradiationF P Li, J B Little, N T Bech-Hansen, et al.
Genomics|April 18, 1998
Construction of a 1.5-Mb bacterial artificial chromosome contig in Xp11.23, a region of high gene contentK M Boycott, R J Zahorchak, C G Summer, et al.
Pageof 6