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D Stoppa-Lyonnet

Showing results (81-90 of 124) with videos related to

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Journal of Medical Genetics|May 31, 2008
Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS familiesG Bougeard, R Sesboüé, S Baert-Desurmont, et al.
British Journal of Cancer|March 7, 2013
Short-term psychological impact of the BRCA1/2 test result in women with breast cancer according to their perceived probability of genetic predisposition to cancerA Brédart, J L Kop, A Depauw, et al.
Cancer Research|May 1, 1998
Mutations at BRCA1: the medullary breast carcinoma revisitedF Eisinger, J Jacquemier, C Charpin, et al.
Familial Cancer|September 16, 2010
Contribution of CDKN2A/P16 ( INK4A ), P14 (ARF), CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanomaB Buecher, M Gauthier-Villars, L Desjardins, et al.
Disease Markers|December 14, 1999
Genetic testing for breast cancer predisposition in 1999: which molecular strategy and which family criteria?D Stoppa-Lyonnet, M Caligo, D Eccles, et al.
Disease Markers|December 14, 1999
Cancer genetics services in EuropeS Hodgson, B Milner, I Brown, et al.
Lancet (London, England)|December 29, 2000
Tamoxifen and risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study. Hereditary Breast Cancer Clinical Study GroupS A Narod, J S Brunet, P Ghadirian, et al.
Gynecologic Oncology Reports|September 20, 2021
Tumor <i>BRCA</i> testing can reveal a high tumor mutational burden related to <i>POLE</i> pathogenic variantsM-C Villy, J Masliah-Planchon, S Melaabi, et al.
American Journal of Medical Genetics|October 27, 1998
Marker segregation information in breast/ovarian cancer genetic counseling: is it still useful? Groupe Génétique et Cancer de la Fédération Nationale des Centres de Lutte Contre le CancerL Essioux, C Girodet, O Sinilnikova, et al.
Neurogenetics|May 15, 2009
Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical managementM Anheim, M Fleury, B Monga, et al.
Pageof 13

Showing results (81-90 of 124) with videos related to

Sort By:
Pageof 13
Journal of Medical Genetics|May 31, 2008
Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS familiesG Bougeard, R Sesboüé, S Baert-Desurmont, et al.
British Journal of Cancer|March 7, 2013
Short-term psychological impact of the BRCA1/2 test result in women with breast cancer according to their perceived probability of genetic predisposition to cancerA Brédart, J L Kop, A Depauw, et al.
Cancer Research|May 1, 1998
Mutations at BRCA1: the medullary breast carcinoma revisitedF Eisinger, J Jacquemier, C Charpin, et al.
Familial Cancer|September 16, 2010
Contribution of CDKN2A/P16 ( INK4A ), P14 (ARF), CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanomaB Buecher, M Gauthier-Villars, L Desjardins, et al.
Disease Markers|December 14, 1999
Genetic testing for breast cancer predisposition in 1999: which molecular strategy and which family criteria?D Stoppa-Lyonnet, M Caligo, D Eccles, et al.
Disease Markers|December 14, 1999
Cancer genetics services in EuropeS Hodgson, B Milner, I Brown, et al.
Lancet (London, England)|December 29, 2000
Tamoxifen and risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study. Hereditary Breast Cancer Clinical Study GroupS A Narod, J S Brunet, P Ghadirian, et al.
Gynecologic Oncology Reports|September 20, 2021
Tumor <i>BRCA</i> testing can reveal a high tumor mutational burden related to <i>POLE</i> pathogenic variantsM-C Villy, J Masliah-Planchon, S Melaabi, et al.
American Journal of Medical Genetics|October 27, 1998
Marker segregation information in breast/ovarian cancer genetic counseling: is it still useful? Groupe Génétique et Cancer de la Fédération Nationale des Centres de Lutte Contre le CancerL Essioux, C Girodet, O Sinilnikova, et al.
Neurogenetics|May 15, 2009
Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical managementM Anheim, M Fleury, B Monga, et al.
Pageof 13