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H Sobol

Showing results (21-30 of 94) with videos related to

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International Journal of Oncology|December 15, 2000
Tamoxifen and breast cancer risk in women harboring a BRCA1 germline mutation: computed efficacy, effectiveness and impactF Eisinger, E Charafe-Jauffret, J Jacquemier, et al.
Journal of Genetic Counseling|May 22, 2013
French professionals in genetic counselor careersC Cordier, N Taris, A De Pauw, et al.
Cytogenetics and Cell Genetics|January 1, 1991
The gene for mannose-binding protein maps to chromosome 10 and is a marker for multiple endocrine neoplasia type 2I Schuffenecker, S A Narod, R A Ezekowitz, et al.
Presse Medicale (Paris, France : 1983)|February 22, 1992
[Cutaneous lesion associated with multiple endocrine neoplasms type 2A (Sipple's syndrome). An early clinical marker]O Chabre, F Labat-Moleur, F Berthod, et al.
Henry Ford Hospital Medical Journal|January 1, 1989
Hereditary medullary thyroid carcinoma: genetic annalysis of three related syndromes. Groupe d'Etude des Tumeurs a CalcitonineH Sobol, S A Narod, I Schuffenecker, et al.
Social Science & Medicine (1982)|January 16, 2004
Prevention and genetic testing for breast cancer: variations in medical decisionsLouise Bouchard, I Blancquaert, F Eisinger, et al.
Presse Medicale (Paris, France : 1983)|December 21, 1991
[Multiple endocrine neoplasms type 2. Recent aspects]P J Guillausseau, C Calmettes, N Feingold, et al.
International Journal of Oncology|May 3, 2011
BRCA1-p53 relationship in hereditary breast cancerH Sobol, D Stoppalyonnet, B Bressacdepaillerets, et al.
Oncology Reports|May 21, 2011
Sublocalization of smallest common regions of deletion on chromosome 17q12-q23 in sporadic primary breast-tumorsM Champeme, S Mazoyer, D Stoppalyonnet, et al.
Cancer Genetics and Cytogenetics|May 22, 1998
Askin tumor and acute myeloid leukemia in a patient with constitutional partial Y disomyM J Mozziconacci, H Sobol, R Costello, et al.
Pageof 10

Showing results (21-30 of 94) with videos related to

Sort By:
Pageof 10
International Journal of Oncology|December 15, 2000
Tamoxifen and breast cancer risk in women harboring a BRCA1 germline mutation: computed efficacy, effectiveness and impactF Eisinger, E Charafe-Jauffret, J Jacquemier, et al.
Journal of Genetic Counseling|May 22, 2013
French professionals in genetic counselor careersC Cordier, N Taris, A De Pauw, et al.
Cytogenetics and Cell Genetics|January 1, 1991
The gene for mannose-binding protein maps to chromosome 10 and is a marker for multiple endocrine neoplasia type 2I Schuffenecker, S A Narod, R A Ezekowitz, et al.
Presse Medicale (Paris, France : 1983)|February 22, 1992
[Cutaneous lesion associated with multiple endocrine neoplasms type 2A (Sipple's syndrome). An early clinical marker]O Chabre, F Labat-Moleur, F Berthod, et al.
Henry Ford Hospital Medical Journal|January 1, 1989
Hereditary medullary thyroid carcinoma: genetic annalysis of three related syndromes. Groupe d'Etude des Tumeurs a CalcitonineH Sobol, S A Narod, I Schuffenecker, et al.
Social Science & Medicine (1982)|January 16, 2004
Prevention and genetic testing for breast cancer: variations in medical decisionsLouise Bouchard, I Blancquaert, F Eisinger, et al.
Presse Medicale (Paris, France : 1983)|December 21, 1991
[Multiple endocrine neoplasms type 2. Recent aspects]P J Guillausseau, C Calmettes, N Feingold, et al.
International Journal of Oncology|May 3, 2011
BRCA1-p53 relationship in hereditary breast cancerH Sobol, D Stoppalyonnet, B Bressacdepaillerets, et al.
Oncology Reports|May 21, 2011
Sublocalization of smallest common regions of deletion on chromosome 17q12-q23 in sporadic primary breast-tumorsM Champeme, S Mazoyer, D Stoppalyonnet, et al.
Cancer Genetics and Cytogenetics|May 22, 1998
Askin tumor and acute myeloid leukemia in a patient with constitutional partial Y disomyM J Mozziconacci, H Sobol, R Costello, et al.
Pageof 10