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C G Mathew

Showing results (31-40 of 129) with videos related to

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Archives of Disease in Childhood|January 1, 1993
A new autosomal recessive anomaly mimicking Fanconi's anaemia phenotypeR D Milner, K A Khallouf, R Gibson, et al.
Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.
Journal of Medical Genetics|September 1, 1995
A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255C P Bennett, A J Barnicoat, F Cotter, et al.
Genes, Chromosomes & Cancer|March 1, 1993
Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2L M Mulligan, E Gardner, B A Smith, et al.
Nucleic Acids Research|October 25, 1991
A MseI polymorphism in exon 48 of the dystrophin geneS C Yau, R G Roberts, D R Bentley, et al.
International Journal of Colorectal Disease|December 31, 1998
The interferon-gamma gene as a positional and functional candidate gene for inflammatory bowel diseaseJ Hampe, B Hermann, S Bridger, et al.
Lancet (London, England)|September 11, 1993
FACC gene mutations and early prenatal diagnosis of Fanconi's anaemiaM Murer-Orlando, J C Llerena, F Birjandi, et al.
British Journal of Haematology|August 1, 1987
Characterization of a new alpha zero thalassaemia defect in the South African populationS Vandenplas, D R Higgs, R D Nicholls, et al.
Biochemical and Biophysical Research Communications|April 27, 1979
A comparison of the high mobility group non-histone chromatin protein HMG 2 in chicken thymus and erythrocytesC G Mathew, G H Goodwin, K Gooderham, et al.
Nucleic Acids Research|February 25, 1988
Styl RFLP recognised by a human IRBP cDNA localised to chromosome 10K S Chin, C G Mathew, S L Fong, et al.
Pageof 13

Showing results (31-40 of 129) with videos related to

Sort By:
Pageof 13
Archives of Disease in Childhood|January 1, 1993
A new autosomal recessive anomaly mimicking Fanconi's anaemia phenotypeR D Milner, K A Khallouf, R Gibson, et al.
Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.
Journal of Medical Genetics|September 1, 1995
A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255C P Bennett, A J Barnicoat, F Cotter, et al.
Genes, Chromosomes & Cancer|March 1, 1993
Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2L M Mulligan, E Gardner, B A Smith, et al.
Nucleic Acids Research|October 25, 1991
A MseI polymorphism in exon 48 of the dystrophin geneS C Yau, R G Roberts, D R Bentley, et al.
International Journal of Colorectal Disease|December 31, 1998
The interferon-gamma gene as a positional and functional candidate gene for inflammatory bowel diseaseJ Hampe, B Hermann, S Bridger, et al.
Lancet (London, England)|September 11, 1993
FACC gene mutations and early prenatal diagnosis of Fanconi's anaemiaM Murer-Orlando, J C Llerena, F Birjandi, et al.
British Journal of Haematology|August 1, 1987
Characterization of a new alpha zero thalassaemia defect in the South African populationS Vandenplas, D R Higgs, R D Nicholls, et al.
Biochemical and Biophysical Research Communications|April 27, 1979
A comparison of the high mobility group non-histone chromatin protein HMG 2 in chicken thymus and erythrocytesC G Mathew, G H Goodwin, K Gooderham, et al.
Nucleic Acids Research|February 25, 1988
Styl RFLP recognised by a human IRBP cDNA localised to chromosome 10K S Chin, C G Mathew, S L Fong, et al.
Pageof 13