Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M R Stratton

Showing results (81-90 of 97) with videos related to

Pageof 10
Sort By:
American Journal of Human Genetics|July 27, 1999
A gene for lymphedema-distichiasis maps to 16q24.3J Mangion, N Rahman, S Mansour, et al.
Nature Genetics|March 1, 1996
Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locusC M Phelan, T R Rebbeck, B L Weber, 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.
Bioinformatics (Oxford, England)|May 9, 2007
AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomesE Dicks, J W Teague, P Stephens, et al.
Oncogene|August 30, 2000
Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22N Rahman, M D Teare, S Seal, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|November 28, 2002
BRCA1 and BRCA2 germline mutations in Sardinian breast cancer families and their implications for genetic counselingG Palmieri, G Palomba, A Cossu, et al.
American Journal of Human Genetics|November 5, 1997
Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancerG R Bignell, F Canzian, M Shayeghi, et al.
Nature Genetics|June 1, 1996
BRCA2 mutations in primary breast and ovarian cancersJ M Lancaster, R Wooster, J Mangion, et al.
Nature|January 15, 1998
A serine/threonine kinase gene defective in Peutz-Jeghers syndromeA Hemminki, D Markie, I Tomlinson, et al.
Cancer Research|September 2, 2000
The frequency of germ-line mutations in the breast cancer predisposition genes BRCA1 and BRCA2 in familial prostate cancer. The Cancer Research Campaign/British Prostate Group United Kingdom Familial Prostate Cancer Study CollaboratorsS A Gayther, K A de Foy, P Harrington, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|July 27, 1999
A gene for lymphedema-distichiasis maps to 16q24.3J Mangion, N Rahman, S Mansour, et al.
Nature Genetics|March 1, 1996
Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locusC M Phelan, T R Rebbeck, B L Weber, 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.
Bioinformatics (Oxford, England)|May 9, 2007
AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomesE Dicks, J W Teague, P Stephens, et al.
Oncogene|August 30, 2000
Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22N Rahman, M D Teare, S Seal, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|November 28, 2002
BRCA1 and BRCA2 germline mutations in Sardinian breast cancer families and their implications for genetic counselingG Palmieri, G Palomba, A Cossu, et al.
American Journal of Human Genetics|November 5, 1997
Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancerG R Bignell, F Canzian, M Shayeghi, et al.
Nature Genetics|June 1, 1996
BRCA2 mutations in primary breast and ovarian cancersJ M Lancaster, R Wooster, J Mangion, et al.
Nature|January 15, 1998
A serine/threonine kinase gene defective in Peutz-Jeghers syndromeA Hemminki, D Markie, I Tomlinson, et al.
Cancer Research|September 2, 2000
The frequency of germ-line mutations in the breast cancer predisposition genes BRCA1 and BRCA2 in familial prostate cancer. The Cancer Research Campaign/British Prostate Group United Kingdom Familial Prostate Cancer Study CollaboratorsS A Gayther, K A de Foy, P Harrington, et al.
Pageof 10