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C G Mathew

Showing results (101-110 of 129) with videos related to

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Annals of Human Genetics|August 28, 2003
Genetic variation at the chromosome 16 chemokine gene cluster: development of a strategy for association studies in complex diseaseS A Fisher, A Moody, M M Mirza, et al.
Oncogene|January 24, 2008
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3J B Wilson, K Yamamoto, A S Marriott, et al.
Genomics|April 1, 1989
Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10R M Landsvater, C G Mathew, B A Smith, et al.
Journal of Medical Genetics|November 13, 2007
Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn diseaseN Wolf, M Quaranta, N J Prescott, et al.
Journal of Medical Genetics|April 16, 1998
Evidence of linkage of the inflammatory bowel disease susceptibility locus on chromosome 16 (IBD1) to ulcerative colitisM M Mirza, J Lee, D Teare, et al.
British Journal of Cancer|March 31, 1999
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3A M Cleton-Jansen, E W Moerland, J C Pronk, et al.
Journal of Medical Genetics|February 24, 2001
Low prevalence of germline BRCA1 mutations in early onset breast cancer without a family historyD Ellis, J Greenman, S Hodgson, et al.
Experimental Dermatology|August 22, 2003
A Crohn's disease-associated insertion polymorphism (3020insC) in the NOD2 gene is not associated with psoriasis vulgaris, palmo-plantar pustular psoriasis or guttate psoriasisC Young, M H Allen, A Cuthbert, et al.
Nature Genetics|August 4, 1999
Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicismQ Waisfisz, N V Morgan, M Savino, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|June 6, 2003
Genetic variation in the IGSF6 gene and lack of association with inflammatory bowel diseaseK King, A Moody, S A Fisher, et al.
Pageof 13

Showing results (101-110 of 129) with videos related to

Sort By:
Pageof 13
Annals of Human Genetics|August 28, 2003
Genetic variation at the chromosome 16 chemokine gene cluster: development of a strategy for association studies in complex diseaseS A Fisher, A Moody, M M Mirza, et al.
Oncogene|January 24, 2008
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3J B Wilson, K Yamamoto, A S Marriott, et al.
Genomics|April 1, 1989
Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10R M Landsvater, C G Mathew, B A Smith, et al.
Journal of Medical Genetics|November 13, 2007
Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn diseaseN Wolf, M Quaranta, N J Prescott, et al.
Journal of Medical Genetics|April 16, 1998
Evidence of linkage of the inflammatory bowel disease susceptibility locus on chromosome 16 (IBD1) to ulcerative colitisM M Mirza, J Lee, D Teare, et al.
British Journal of Cancer|March 31, 1999
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3A M Cleton-Jansen, E W Moerland, J C Pronk, et al.
Journal of Medical Genetics|February 24, 2001
Low prevalence of germline BRCA1 mutations in early onset breast cancer without a family historyD Ellis, J Greenman, S Hodgson, et al.
Experimental Dermatology|August 22, 2003
A Crohn's disease-associated insertion polymorphism (3020insC) in the NOD2 gene is not associated with psoriasis vulgaris, palmo-plantar pustular psoriasis or guttate psoriasisC Young, M H Allen, A Cuthbert, et al.
Nature Genetics|August 4, 1999
Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicismQ Waisfisz, N V Morgan, M Savino, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|June 6, 2003
Genetic variation in the IGSF6 gene and lack of association with inflammatory bowel diseaseK King, A Moody, S A Fisher, et al.
Pageof 13