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Optics Express
|
January 4, 2011
Loss engineered slow light waveguides
L O'Faolain, S A Schulz, D M Beggs, et al.
Nature Genetics
|
November 1, 1996
A polymorphic stop codon in BRCA2
S 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 France
O 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 correlation
S 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 study
S L Neuhausen, S Mazoyer, L Friedman, et al.
Clinical Genetics
|
April 5, 2016
Refining the phenotypical and mutational spectrum of Taybi-Linder syndrome
A Putoux, A Alqahtani, L Pinson, et al.
Journal of Medical Genetics
|
September 5, 2006
The contribution of germline rearrangements to the spectrum of BRCA2 mutations
F 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 study
A Jakubowska, D Rozkrut, A Antoniou, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 38) with videos related to
Sort By:
Page
of 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 waveguides
L O'Faolain, S A Schulz, D M Beggs, et al.
Nature Genetics
|
November 1, 1996
A polymorphic stop codon in BRCA2
S 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 France
O 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 correlation
S 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 study
S L Neuhausen, S Mazoyer, L Friedman, et al.
Clinical Genetics
|
April 5, 2016
Refining the phenotypical and mutational spectrum of Taybi-Linder syndrome
A Putoux, A Alqahtani, L Pinson, et al.
Journal of Medical Genetics
|
September 5, 2006
The contribution of germline rearrangements to the spectrum of BRCA2 mutations
F 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 study
A Jakubowska, D Rozkrut, A Antoniou, et al.
Page
of 4