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Cédrick Lefol

Showing results (1-10 of 8) with videos related to

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Human Mutation|February 19, 2009
Quantitative PCR high-resolution melting (qPCR-HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application to MLH1 germline mutations in Lynch syndromeEtienne Rouleau, Cédrick Lefol, Violaine Bourdon, et al.
Journal of Medical Genetics|January 30, 2020
Characterisation of heterozygous <i>PMS2</i> variants in French patients with Lynch syndromeQing Wang, Julie Leclerc, Gaëlle Bougeard, et al.
BMC Medical Genetics|September 24, 2011
An entire exon 3 germ-line rearrangement in the BRCA2 gene: pathogenic relevance of exon 3 deletion in breast cancer predispositionDanièle Muller, Etienne Rouleau, Inès Schultz, et al.
Genes, Chromosomes & Cancer|March 31, 2015
Dismantling papillary renal cell carcinoma classification: The heterogeneity of genetic profiles suggests several independent diseasesAlexandre Marsaud, Bérengère Dadone, Damien Ambrosetti, et al.
Human Mutation|April 17, 2012
Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variantsClaude Houdayer, Virginie Caux-Moncoutier, Sophie Krieger, et al.
Oncotarget|May 1, 2018
Full in-frame exon 3 skipping of <i>BRCA2</i> confers high risk of breast and/or ovarian cancerSandrine M Caputo, Mélanie Léone, Francesca Damiola, et al.
Breast Cancer Research : BCR|May 1, 2015
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriersSophie Blein, Claire Bardel, Vincent Danjean, et al.
Breast Cancer Research : BCR|April 29, 2015
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriersKaroline B Kuchenbaecker, Susan L Neuhausen, Mark Robson, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Human Mutation|February 19, 2009
Quantitative PCR high-resolution melting (qPCR-HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application to MLH1 germline mutations in Lynch syndromeEtienne Rouleau, Cédrick Lefol, Violaine Bourdon, et al.
Journal of Medical Genetics|January 30, 2020
Characterisation of heterozygous <i>PMS2</i> variants in French patients with Lynch syndromeQing Wang, Julie Leclerc, Gaëlle Bougeard, et al.
BMC Medical Genetics|September 24, 2011
An entire exon 3 germ-line rearrangement in the BRCA2 gene: pathogenic relevance of exon 3 deletion in breast cancer predispositionDanièle Muller, Etienne Rouleau, Inès Schultz, et al.
Genes, Chromosomes & Cancer|March 31, 2015
Dismantling papillary renal cell carcinoma classification: The heterogeneity of genetic profiles suggests several independent diseasesAlexandre Marsaud, Bérengère Dadone, Damien Ambrosetti, et al.
Human Mutation|April 17, 2012
Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variantsClaude Houdayer, Virginie Caux-Moncoutier, Sophie Krieger, et al.
Oncotarget|May 1, 2018
Full in-frame exon 3 skipping of <i>BRCA2</i> confers high risk of breast and/or ovarian cancerSandrine M Caputo, Mélanie Léone, Francesca Damiola, et al.
Breast Cancer Research : BCR|May 1, 2015
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriersSophie Blein, Claire Bardel, Vincent Danjean, et al.
Breast Cancer Research : BCR|April 29, 2015
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriersKaroline B Kuchenbaecker, Susan L Neuhausen, Mark Robson, et al.
Pageof 1