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S Mazoyer

Showing results (31-40 of 38) with videos related to

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Optics Express|January 4, 2011
Loss engineered slow light waveguidesL O'Faolain, S A Schulz, D M Beggs, et al.
Nature Genetics|November 1, 1996
A polymorphic stop codon in BRCA2S Mazoyer, A M Dunning, O Serova, et al.
American Journal of Human Genetics|May 1, 1997
BRCA2 mutations in hereditary breast and ovarian cancer in FranceO M Serova-Sinilnikova, L Boutrand, D Stoppa-Lyonnet, et al.
Nature Genetics|December 1, 1995
Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlationS A Gayther, W Warren, S Mazoyer, 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.
Clinical Genetics|April 5, 2016
Refining the phenotypical and mutational spectrum of Taybi-Linder syndromeA Putoux, A Alqahtani, L Pinson, et al.
Journal of Medical Genetics|September 5, 2006
The contribution of germline rearrangements to the spectrum of BRCA2 mutationsF Casilli, I Tournier, O M Sinilnikova, et al.
British Journal of Cancer|June 7, 2012
Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter studyA Jakubowska, D Rozkrut, A Antoniou, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Optics Express|January 4, 2011
Loss engineered slow light waveguidesL O'Faolain, S A Schulz, D M Beggs, et al.
Nature Genetics|November 1, 1996
A polymorphic stop codon in BRCA2S Mazoyer, A M Dunning, O Serova, et al.
American Journal of Human Genetics|May 1, 1997
BRCA2 mutations in hereditary breast and ovarian cancer in FranceO M Serova-Sinilnikova, L Boutrand, D Stoppa-Lyonnet, et al.
Nature Genetics|December 1, 1995
Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlationS A Gayther, W Warren, S Mazoyer, 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.
Clinical Genetics|April 5, 2016
Refining the phenotypical and mutational spectrum of Taybi-Linder syndromeA Putoux, A Alqahtani, L Pinson, et al.
Journal of Medical Genetics|September 5, 2006
The contribution of germline rearrangements to the spectrum of BRCA2 mutationsF Casilli, I Tournier, O M Sinilnikova, et al.
British Journal of Cancer|June 7, 2012
Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter studyA Jakubowska, D Rozkrut, A Antoniou, et al.
Pageof 4