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

D G EVANS

Showing results (371-380 of 392) with videos related to

Pageof 40
Sort By:
The British Journal of Surgery|May 27, 2021
European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and genderT T Seppälä, A Latchford, I Negoi, et al.
American Journal of Medical Genetics. Part A|October 21, 2016
Creation of an international registry to support discovery in schwannomatosisK L Ostrow, A L Bergner, J Blakeley, et al.
British Journal of Cancer|October 4, 2006
Cost-effectiveness of screening with contrast enhanced magnetic resonance imaging vs X-ray mammography of women at a high familial risk of breast cancerI Griebsch, J Brown, C Boggis, et al.
Gut|June 3, 2008
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3A R Dallosso, S Dolwani, N Jones, et al.
American Journal of Human Genetics|December 13, 2006
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlationM Upadhyaya, S M Huson, M Davies, et al.
Breast (Edinburgh, Scotland)|January 21, 2004
Rationale for a national multi-centre study of magnetic resonance imaging screening in women at genetic risk of breast cancerJ Brown, A Coulthard, A K Dixon, et al.
Breast (Edinburgh, Scotland)|January 21, 2004
Protocol for a national multi-centre study of magnetic resonance imaging screening in women at genetic risk of breast cancerJ Brown, A Coulthard, A K Dixon, et al.
Human Genetics|September 12, 2000
Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13M Takahashi, E Rapley, P J Biggs, et al.
Nature Genetics|June 3, 2000
Identification of the familial cylindromatosis tumour-suppressor geneG R Bignell, W Warren, S Seal, et al.
Journal of Neurogenetics|September 19, 2000
Advances in neurofibromatosis 2 (NF2): a workshop reportD J Lim, A E Rubenstein, D G Evans, et al.
Pageof 40

Showing results (371-380 of 392) with videos related to

Sort By:
Pageof 40
The British Journal of Surgery|May 27, 2021
European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and genderT T Seppälä, A Latchford, I Negoi, et al.
American Journal of Medical Genetics. Part A|October 21, 2016
Creation of an international registry to support discovery in schwannomatosisK L Ostrow, A L Bergner, J Blakeley, et al.
British Journal of Cancer|October 4, 2006
Cost-effectiveness of screening with contrast enhanced magnetic resonance imaging vs X-ray mammography of women at a high familial risk of breast cancerI Griebsch, J Brown, C Boggis, et al.
Gut|June 3, 2008
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3A R Dallosso, S Dolwani, N Jones, et al.
American Journal of Human Genetics|December 13, 2006
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlationM Upadhyaya, S M Huson, M Davies, et al.
Breast (Edinburgh, Scotland)|January 21, 2004
Rationale for a national multi-centre study of magnetic resonance imaging screening in women at genetic risk of breast cancerJ Brown, A Coulthard, A K Dixon, et al.
Breast (Edinburgh, Scotland)|January 21, 2004
Protocol for a national multi-centre study of magnetic resonance imaging screening in women at genetic risk of breast cancerJ Brown, A Coulthard, A K Dixon, et al.
Human Genetics|September 12, 2000
Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13M Takahashi, E Rapley, P J Biggs, et al.
Nature Genetics|June 3, 2000
Identification of the familial cylindromatosis tumour-suppressor geneG R Bignell, W Warren, S Seal, et al.
Journal of Neurogenetics|September 19, 2000
Advances in neurofibromatosis 2 (NF2): a workshop reportD J Lim, A E Rubenstein, D G Evans, et al.
Pageof 40