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D Stoppa-Lyonnet

Showing results (101-110 of 124) with videos related to

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Bulletin Du Cancer|September 16, 2009
[Cancer genetics: estimation of the needs of the population in France for the next ten years]C Bonaïti-Pellié, N Andrieu, P Arveux, et al.
British Journal of Cancer|September 30, 2010
Establishment and characterisation of a new breast cancer xenograft obtained from a woman carrying a germline BRCA2 mutationL de Plater, A Laugé, C Guyader, et al.
Breast Cancer Research and Treatment|December 14, 2017
Assessment of the functional impact of germline BRCA1/2 variants located in non-coding regions in families with breast and/or ovarian cancer predispositionE Santana Dos Santos, S M Caputo, L Castera, et al.
Annales De Dermatologie Et De Venereologie|January 21, 2015
[Recommendations for genetic testing and management of individuals genetically at-risk of cutaneous melanoma]M-F Avril, P Bahadoran, O Cabaret, et al.
Journal of Medical Genetics|October 3, 1999
Linkage analysis of 56 multiplex families excludes the Cowden disease gene PTEN as a major contributor to familial breast cancerY Y Shugart, C Cour, H Renard, et al.
Journal of Neurology|August 28, 2010
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arraysD H'mida-Ben Brahim, A M'zahem, M Assoum, et al.
Disease Markers|December 14, 1999
Guidelines for follow-up of women at high risk for inherited breast cancer: consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast CancerP Møller, G Evans, N Haites, et al.
Breast Cancer Research and Treatment|August 27, 2013
Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic testsP Pujol, D Stoppa Lyonnet, T Frebourg, et al.
Breast Cancer Research and Treatment|April 6, 2012
Rare germline large rearrangements in the BRCA1/2 genes and eight candidate genes in 472 patients with breast cancer predispositionE Rouleau, B Jesson, A Briaux, et al.
American Journal of Human Genetics|February 1, 1996
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international studyS L Neuhausen, S Mazoyer, L Friedman, et al.
Pageof 13

Showing results (101-110 of 124) with videos related to

Sort By:
Pageof 13
Bulletin Du Cancer|September 16, 2009
[Cancer genetics: estimation of the needs of the population in France for the next ten years]C Bonaïti-Pellié, N Andrieu, P Arveux, et al.
British Journal of Cancer|September 30, 2010
Establishment and characterisation of a new breast cancer xenograft obtained from a woman carrying a germline BRCA2 mutationL de Plater, A Laugé, C Guyader, et al.
Breast Cancer Research and Treatment|December 14, 2017
Assessment of the functional impact of germline BRCA1/2 variants located in non-coding regions in families with breast and/or ovarian cancer predispositionE Santana Dos Santos, S M Caputo, L Castera, et al.
Annales De Dermatologie Et De Venereologie|January 21, 2015
[Recommendations for genetic testing and management of individuals genetically at-risk of cutaneous melanoma]M-F Avril, P Bahadoran, O Cabaret, et al.
Journal of Medical Genetics|October 3, 1999
Linkage analysis of 56 multiplex families excludes the Cowden disease gene PTEN as a major contributor to familial breast cancerY Y Shugart, C Cour, H Renard, et al.
Journal of Neurology|August 28, 2010
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arraysD H'mida-Ben Brahim, A M'zahem, M Assoum, et al.
Disease Markers|December 14, 1999
Guidelines for follow-up of women at high risk for inherited breast cancer: consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast CancerP Møller, G Evans, N Haites, et al.
Breast Cancer Research and Treatment|August 27, 2013
Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic testsP Pujol, D Stoppa Lyonnet, T Frebourg, et al.
Breast Cancer Research and Treatment|April 6, 2012
Rare germline large rearrangements in the BRCA1/2 genes and eight candidate genes in 472 patients with breast cancer predispositionE Rouleau, B Jesson, A Briaux, et al.
American Journal of Human Genetics|February 1, 1996
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international studyS L Neuhausen, S Mazoyer, L Friedman, et al.
Pageof 13