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Annales D'Endocrinologie
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April 6, 1999
[INSERM-FNCLCC collective expert's report. Recommendations for management of women having a genetic risk of developing breast and/or ovarian cancer. National Federation of Centers of the Fight Against Cancer]
F Eisinger, N Alby, A Bremond, et al.
Annales De Genetique
|
April 24, 1999
[INSERM-FNCLCC collective expertise. Recommendations for medical management of women with genetic risk of developing breast and/or ovarian cancer]
F Eisinger, N Alby, A Bremond, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
November 18, 1998
Recommendations for medical management of hereditary breast and ovarian cancer: the French National Ad Hoc Committee
F Eisinger, N Alby, A Bremond, et al.
Bulletin Du Cancer
|
April 22, 1999
[Inserm ad hoc committee: Recommendations for the management of women with a genetic risk for developing cancer of the breast and/or the ovary]
F Eisinger, N Alby, A Bremond, et al.
Disease Markers
|
December 14, 1999
Insurance implications for individuals with a high risk of breast and ovarian cancer in Europe
P J Morrison, C M Steel, H F Vasen, et al.
Gene
|
August 5, 2006
Structural organization and expression of human MTUS1, a candidate 8p22 tumor suppressor gene encoding a family of angiotensin II AT2 receptor-interacting proteins, ATIP
M Di Benedetto, I Bièche, F Deshayes, et al.
Oncogene
|
September 13, 2003
Multiple molecular mechanisms contribute to radiation sensitivity in mantle cell lymphoma
R M'kacher, A Bennaceur, F Farace, et al.
Neuromolecular Medicine
|
January 17, 2013
Molecular defects in Moroccan patients with ataxia-telangiectasia
L Jeddane, F Ailal, C Dubois-d'Enghien, et al.
American Journal of Human Genetics
|
May 1, 1997
BRCA2 mutations in hereditary breast and ovarian cancer in France
O M Serova-Sinilnikova, L Boutrand, D Stoppa-Lyonnet, et al.
Pediatric Blood & Cancer
|
August 24, 2013
Malformations, genetic abnormalities, and Wilms tumor
S Dumoucel, M Gauthier-Villars, D Stoppa-Lyonnet, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 124) with videos related to
Sort By:
Page
of 13
Annales D'Endocrinologie
|
April 6, 1999
[INSERM-FNCLCC collective expert's report. Recommendations for management of women having a genetic risk of developing breast and/or ovarian cancer. National Federation of Centers of the Fight Against Cancer]
F Eisinger, N Alby, A Bremond, et al.
Annales De Genetique
|
April 24, 1999
[INSERM-FNCLCC collective expertise. Recommendations for medical management of women with genetic risk of developing breast and/or ovarian cancer]
F Eisinger, N Alby, A Bremond, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
November 18, 1998
Recommendations for medical management of hereditary breast and ovarian cancer: the French National Ad Hoc Committee
F Eisinger, N Alby, A Bremond, et al.
Bulletin Du Cancer
|
April 22, 1999
[Inserm ad hoc committee: Recommendations for the management of women with a genetic risk for developing cancer of the breast and/or the ovary]
F Eisinger, N Alby, A Bremond, et al.
Disease Markers
|
December 14, 1999
Insurance implications for individuals with a high risk of breast and ovarian cancer in Europe
P J Morrison, C M Steel, H F Vasen, et al.
Gene
|
August 5, 2006
Structural organization and expression of human MTUS1, a candidate 8p22 tumor suppressor gene encoding a family of angiotensin II AT2 receptor-interacting proteins, ATIP
M Di Benedetto, I Bièche, F Deshayes, et al.
Oncogene
|
September 13, 2003
Multiple molecular mechanisms contribute to radiation sensitivity in mantle cell lymphoma
R M'kacher, A Bennaceur, F Farace, et al.
Neuromolecular Medicine
|
January 17, 2013
Molecular defects in Moroccan patients with ataxia-telangiectasia
L Jeddane, F Ailal, C Dubois-d'Enghien, et al.
American Journal of Human Genetics
|
May 1, 1997
BRCA2 mutations in hereditary breast and ovarian cancer in France
O M Serova-Sinilnikova, L Boutrand, D Stoppa-Lyonnet, et al.
Pediatric Blood & Cancer
|
August 24, 2013
Malformations, genetic abnormalities, and Wilms tumor
S Dumoucel, M Gauthier-Villars, D Stoppa-Lyonnet, et al.
Page
of 13