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C G Mathew

Showing results (51-60 of 129) with videos related to

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Human Genetics|January 1, 1985
Two new polymorphic markers in the human pro alpha 2(1) collagen geneD K Brebner, A F Grobler-Rabie, A J Bester, et al.
Gut|August 13, 2004
Genetic association between EPHX1 and Crohn's disease: population stratification, genotyping error, or random chance?A P Cuthbert, S A Fisher, C M Lewis, et al.
British Journal of Haematology|June 1, 1996
Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutationsI Dokal, A Chase, N V Morgan, et al.
Journal of Medical Genetics|July 31, 2007
Estimating risks of common complex diseases across genetic and environmental factors: the example of Crohn diseaseC M Lewis, S C L Whitwell, A Forbes, et al.
Human Heredity|January 1, 1990
Minisatellite DNA profiles: rapid sample identification in linkage analysisH Telenius, J Clark, E Marcus, et al.
Acta Haematologica|January 1, 1985
Incidence of Hb Barts and alpha-thalassaemia genotypes in a South African populationJ Rousseau, C G Mathew, J S Rees, et al.
Breast Cancer Research and Treatment|January 8, 2025
Application of genetic testing criteria for hereditary breast cancer in South AfricaT S Osler, M Schoeman, W J S Pretorius, et al.
The EMBO Journal|July 1, 1985
Detection of a high frequency RsaI polymorphism in the human pro alpha 2(I) collagen gene which is linked to an autosomal dominant form of osteogenesis imperfectaA F Grobler-Rabie, G Wallis, D K Brebner, et al.
Acta Haematologica|January 1, 1984
Haemoglobin E variants: a clinical, haematological and biosynthetic study of 4 South African familiesA R Bird, K Wood, F Leisegang, et al.
Gut|July 13, 2005
No association of the NFKB1 promoter polymorphism with ulcerative colitis in a British case control cohortM M Mirza, S A Fisher, C Onnie, et al.
Pageof 13

Showing results (51-60 of 129) with videos related to

Sort By:
Pageof 13
Human Genetics|January 1, 1985
Two new polymorphic markers in the human pro alpha 2(1) collagen geneD K Brebner, A F Grobler-Rabie, A J Bester, et al.
Gut|August 13, 2004
Genetic association between EPHX1 and Crohn's disease: population stratification, genotyping error, or random chance?A P Cuthbert, S A Fisher, C M Lewis, et al.
British Journal of Haematology|June 1, 1996
Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutationsI Dokal, A Chase, N V Morgan, et al.
Journal of Medical Genetics|July 31, 2007
Estimating risks of common complex diseases across genetic and environmental factors: the example of Crohn diseaseC M Lewis, S C L Whitwell, A Forbes, et al.
Human Heredity|January 1, 1990
Minisatellite DNA profiles: rapid sample identification in linkage analysisH Telenius, J Clark, E Marcus, et al.
Acta Haematologica|January 1, 1985
Incidence of Hb Barts and alpha-thalassaemia genotypes in a South African populationJ Rousseau, C G Mathew, J S Rees, et al.
Breast Cancer Research and Treatment|January 8, 2025
Application of genetic testing criteria for hereditary breast cancer in South AfricaT S Osler, M Schoeman, W J S Pretorius, et al.
The EMBO Journal|July 1, 1985
Detection of a high frequency RsaI polymorphism in the human pro alpha 2(I) collagen gene which is linked to an autosomal dominant form of osteogenesis imperfectaA F Grobler-Rabie, G Wallis, D K Brebner, et al.
Acta Haematologica|January 1, 1984
Haemoglobin E variants: a clinical, haematological and biosynthetic study of 4 South African familiesA R Bird, K Wood, F Leisegang, et al.
Gut|July 13, 2005
No association of the NFKB1 promoter polymorphism with ulcerative colitis in a British case control cohortM M Mirza, S A Fisher, C Onnie, et al.
Pageof 13