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

K Tsioupra

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Annals of Human Genetics|January 1, 1995
Haplotype comparison in fresh mutation cases of adenomatous polyposis coli due to deletion AAAGA at codon 1309J D Delhanty, K Tsioupra
Clinical Genetics|July 1, 1990
Chromosome breakage in lymphocytes from members of cancer families showing autosomal dominant inheritanceM N Khouzam, K Tsioupra, J D Delhanty
Journal of Medical Genetics|July 1, 1995
Rapid detection of rare variants and common polymorphisms in the APC gene by PCR-SSCP for presymptomatic diagnosis and showing allele lossS A Gayther, R Sud, D Wells, et al.
Human Mutation|January 1, 1996
Four novel germline mutations of the APC geneD Wells, P Chapman, J C Landgrebe, et al.
Lancet (London, England)|September 3, 1988
Familial polyposis coliM A Aldred, M Rees, K Tsioupra, et al.
Disease Markers|June 1, 1988
Spontaneous and induced chromosome damage in lymphocytes of medullary thyroid carcinoma patients and their family membersK Tsioupra, L F West, M B Davis, et al.
Journal of Medical Genetics|October 1, 1991
Linkage analysis in adenomatous polyposis coli: the use of four closely linked DNA probes in 20 UK familiesM B Cachon-Gonzalez, J D Delhanty, J Burn, et al.
Journal of the Royal Society of Medicine|August 1, 1990
Familial Raynaud's phenomenon and localized scleroderma associated with essential telangiectasia and cytogenetic abnormalitiesC B Bunker, D Atherton, O P Gray, et al.
Human Molecular Genetics|January 1, 1994
Regionally clustered APC mutations are associated with a severe phenotype and occur at a high frequency in new mutation cases of adenomatous polyposis coliS A Gayther, D Wells, S B SenGupta, et al.
Journal of Medical Genetics|May 1, 1991
The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculationsJ Burn, P Chapman, J Delhanty, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Annals of Human Genetics|January 1, 1995
Haplotype comparison in fresh mutation cases of adenomatous polyposis coli due to deletion AAAGA at codon 1309J D Delhanty, K Tsioupra
Clinical Genetics|July 1, 1990
Chromosome breakage in lymphocytes from members of cancer families showing autosomal dominant inheritanceM N Khouzam, K Tsioupra, J D Delhanty
Journal of Medical Genetics|July 1, 1995
Rapid detection of rare variants and common polymorphisms in the APC gene by PCR-SSCP for presymptomatic diagnosis and showing allele lossS A Gayther, R Sud, D Wells, et al.
Human Mutation|January 1, 1996
Four novel germline mutations of the APC geneD Wells, P Chapman, J C Landgrebe, et al.
Lancet (London, England)|September 3, 1988
Familial polyposis coliM A Aldred, M Rees, K Tsioupra, et al.
Disease Markers|June 1, 1988
Spontaneous and induced chromosome damage in lymphocytes of medullary thyroid carcinoma patients and their family membersK Tsioupra, L F West, M B Davis, et al.
Journal of Medical Genetics|October 1, 1991
Linkage analysis in adenomatous polyposis coli: the use of four closely linked DNA probes in 20 UK familiesM B Cachon-Gonzalez, J D Delhanty, J Burn, et al.
Journal of the Royal Society of Medicine|August 1, 1990
Familial Raynaud's phenomenon and localized scleroderma associated with essential telangiectasia and cytogenetic abnormalitiesC B Bunker, D Atherton, O P Gray, et al.
Human Molecular Genetics|January 1, 1994
Regionally clustered APC mutations are associated with a severe phenotype and occur at a high frequency in new mutation cases of adenomatous polyposis coliS A Gayther, D Wells, S B SenGupta, et al.
Journal of Medical Genetics|May 1, 1991
The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculationsJ Burn, P Chapman, J Delhanty, et al.
Pageof 2