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O Cabaret

Showing results (1-10 of 7) with videos related to

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Journal of Clinical Microbiology|July 18, 2008
Two unusual occurrences of trichomoniasis: rapid species identification by PCRA P Bellanger, O Cabaret, J M Costa, et al.
Clinical Pharmacology and Therapeutics|November 26, 2010
Effect of NFE2L2 genetic polymorphism on the association between oral estrogen therapy and the risk of venous thromboembolism in postmenopausal womenJ Bouligand, O Cabaret, M Canonico, et al.
Clinical Genetics|August 1, 2014
Germline BAP1 mutations predispose also to multiple basal cell carcinomasA de la Fouchardière, O Cabaret, L Savin, et al.
Journal of Medical Genetics|February 22, 2014
Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D)H F A Vasen, Z Ghorbanoghli, F Bourdeaut, 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.
Digestive Diseases and Sciences|October 31, 2022
The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer PatientsM Baz, V Gondran-Teiller, B Bressac, et al.
Journal of Medical Genetics|August 31, 2015
Constitutional mismatch repair deficiency syndrome: clinical description in a French cohortN Lavoine, C Colas, M Muleris, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Journal of Clinical Microbiology|July 18, 2008
Two unusual occurrences of trichomoniasis: rapid species identification by PCRA P Bellanger, O Cabaret, J M Costa, et al.
Clinical Pharmacology and Therapeutics|November 26, 2010
Effect of NFE2L2 genetic polymorphism on the association between oral estrogen therapy and the risk of venous thromboembolism in postmenopausal womenJ Bouligand, O Cabaret, M Canonico, et al.
Clinical Genetics|August 1, 2014
Germline BAP1 mutations predispose also to multiple basal cell carcinomasA de la Fouchardière, O Cabaret, L Savin, et al.
Journal of Medical Genetics|February 22, 2014
Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D)H F A Vasen, Z Ghorbanoghli, F Bourdeaut, 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.
Digestive Diseases and Sciences|October 31, 2022
The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer PatientsM Baz, V Gondran-Teiller, B Bressac, et al.
Journal of Medical Genetics|August 31, 2015
Constitutional mismatch repair deficiency syndrome: clinical description in a French cohortN Lavoine, C Colas, M Muleris, et al.
Pageof 1