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C G Mathew

Showing results (121-130 of 129) with videos related to

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Genomics|June 20, 1998
Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancerS A Whitmore, J Crawford, S Apostolou, et al.
Lancet (London, England)|June 27, 2001
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populationsJ Hampe, A Cuthbert, P J Croucher, et al.
American Journal of Human Genetics|March 3, 1999
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohortJ Hampe, S Schreiber, S H Shaw, et al.
Genomics|October 29, 1998
Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancerS A Whitmore, C Settasatian, J Crawford, et al.
Blood|December 9, 2000
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research GroupL Faivre, P Guardiola, C Lewis, et al.
American Journal of Human Genetics|September 23, 2000
Isolation of a cDNA representing the Fanconi anemia complementation group E geneJ P de Winter, F Léveillé, C G van Berkel, et al.
Human Mutation|January 1, 1996
Novel mutations and polymorphisms in the Fanconi anemia group C geneR A Gibson, N V Morgan, L H Goldstein, et al.
Mucosal Immunology|November 2, 2017
NOX1 loss-of-function genetic variants in patients with inflammatory bowel diseaseT Schwerd, R V Bryant, S Pandey, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 16, 2017
International cancer seminars: a focus on esophageal squamous cell carcinomaG Murphy, V McCormack, B Abedi-Ardekani, et al.
Pageof 13

Showing results (121-130 of 129) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 129 results.
Genomics|June 20, 1998
Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancerS A Whitmore, J Crawford, S Apostolou, et al.
Lancet (London, England)|June 27, 2001
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populationsJ Hampe, A Cuthbert, P J Croucher, et al.
American Journal of Human Genetics|March 3, 1999
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohortJ Hampe, S Schreiber, S H Shaw, et al.
Genomics|October 29, 1998
Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancerS A Whitmore, C Settasatian, J Crawford, et al.
Blood|December 9, 2000
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research GroupL Faivre, P Guardiola, C Lewis, et al.
American Journal of Human Genetics|September 23, 2000
Isolation of a cDNA representing the Fanconi anemia complementation group E geneJ P de Winter, F Léveillé, C G van Berkel, et al.
Human Mutation|January 1, 1996
Novel mutations and polymorphisms in the Fanconi anemia group C geneR A Gibson, N V Morgan, L H Goldstein, et al.
Mucosal Immunology|November 2, 2017
NOX1 loss-of-function genetic variants in patients with inflammatory bowel diseaseT Schwerd, R V Bryant, S Pandey, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 16, 2017
International cancer seminars: a focus on esophageal squamous cell carcinomaG Murphy, V McCormack, B Abedi-Ardekani, et al.
Pageof 13