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 F Callen

Showing results (171-180 of 195) with videos related to

Pageof 20
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1993
Refined genetic mapping of juvenile-onset neuronal ceroid-lipofuscinosis on chromosome 16H M Mitchison, R E Williams, T R McKay, et al.
Genomics|May 1, 1993
Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite lociH M Mitchison, A D Thompson, J C Mulley, et al.
Genomics|August 1, 1992
High-resolution cytogenetic-based physical map of human chromosome 16D F Callen, N A Doggett, R L Stallings, et al.
Science (New York, N.Y.)|December 8, 1989
A new DNA marker tightly linked to the fragile X locus (FRAXA)G K Suthers, D F Callen, V J Hyland, et al.
Genomics|September 20, 1995
YAC and cosmid contigs spanning the Batten disease (CLN3) region at 16p12.1-p11.2I E Järvelä, H M Mitchison, A M O'Rawe, et al.
Human Genetics|August 14, 2001
Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the geneR Bell, G Brice, A H Child, et al.
Oncogene|July 17, 2012
Mutant p53 drives invasion in breast tumors through up-regulation of miR-155P M Neilsen, J E Noll, S Mattiske, et al.
Annals of Human Genetics|January 30, 1999
Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16J A Cavanaugh, D F Callen, S R Wilson, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 3, 2001
A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticumL Cai, A Lumsden, U P Guenther, et al.
British Journal of Cancer|March 31, 1999
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3A M Cleton-Jansen, E W Moerland, J C Pronk, et al.
Pageof 20

Showing results (171-180 of 195) with videos related to

Sort By:
Pageof 20
Journal of Inherited Metabolic Disease|January 1, 1993
Refined genetic mapping of juvenile-onset neuronal ceroid-lipofuscinosis on chromosome 16H M Mitchison, R E Williams, T R McKay, et al.
Genomics|May 1, 1993
Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite lociH M Mitchison, A D Thompson, J C Mulley, et al.
Genomics|August 1, 1992
High-resolution cytogenetic-based physical map of human chromosome 16D F Callen, N A Doggett, R L Stallings, et al.
Science (New York, N.Y.)|December 8, 1989
A new DNA marker tightly linked to the fragile X locus (FRAXA)G K Suthers, D F Callen, V J Hyland, et al.
Genomics|September 20, 1995
YAC and cosmid contigs spanning the Batten disease (CLN3) region at 16p12.1-p11.2I E Järvelä, H M Mitchison, A M O'Rawe, et al.
Human Genetics|August 14, 2001
Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the geneR Bell, G Brice, A H Child, et al.
Oncogene|July 17, 2012
Mutant p53 drives invasion in breast tumors through up-regulation of miR-155P M Neilsen, J E Noll, S Mattiske, et al.
Annals of Human Genetics|January 30, 1999
Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16J A Cavanaugh, D F Callen, S R Wilson, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 3, 2001
A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticumL Cai, A Lumsden, U P Guenther, et al.
British Journal of Cancer|March 31, 1999
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3A M Cleton-Jansen, E W Moerland, J C Pronk, et al.
Pageof 20