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 W Cox

Showing results (151-160 of 223) with videos related to

Pageof 23
Sort By:
Prenatal Diagnosis|March 1, 2000
Haplotype association and mutation analysis of the transglutaminase 1 gene for prenatal exclusion of lamellar ichthyosisM Pigg, T Gedde-Dahl, D W Cox, et al.
The Journal of Pediatrics|November 4, 2000
Severe hepatic Wilson's disease in preschool-aged childrenD C Wilson, M J Phillips, D W Cox, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 4, 2000
Comparative mapping of human Chromosome 14q11.2-q13 genes with mouse homologous gene regionsD Kamnasaran, P C O'Brien, M A Ferguson-Smith, et al.
Lancet (London, England)|July 28, 1979
Severe combined immune-deficiency disease in patient with alpha 1-antitrypsin deficiencyE W Gelfand, D W Cox, M T Lin, et al.
American Journal of Human Genetics|May 1, 1995
Wilson disease in Iceland: a clinical and genetic studyG R Thomas, O Jensson, G Gudmundsson, et al.
Human Molecular Genetics|January 1, 1993
Polymorphism of the protein C inhibitor (PCI) gene on chromosome 14K J Ashbourne, B C Byth, J C Meijers, et al.
Human Mutation|August 10, 2005
Twenty-four novel mutations in Wilson disease patients of predominantly European ancestryD W Cox, L Prat, J M Walshe, et al.
Genomics|August 10, 1995
Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8V Reed, P Williamson, P C Bull, et al.
American Journal of Human Genetics|June 1, 1989
In-frame single codon deletion in the Mmalton deficiency allele of alpha 1-antitrypsinG C Fraizer, T R Harrold, M H Hofker, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1983
Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locusP S Linsley, N T Bech-Hansen, L Siminovitch, et al.
Pageof 23

Showing results (151-160 of 223) with videos related to

Sort By:
Pageof 23
Prenatal Diagnosis|March 1, 2000
Haplotype association and mutation analysis of the transglutaminase 1 gene for prenatal exclusion of lamellar ichthyosisM Pigg, T Gedde-Dahl, D W Cox, et al.
The Journal of Pediatrics|November 4, 2000
Severe hepatic Wilson's disease in preschool-aged childrenD C Wilson, M J Phillips, D W Cox, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 4, 2000
Comparative mapping of human Chromosome 14q11.2-q13 genes with mouse homologous gene regionsD Kamnasaran, P C O'Brien, M A Ferguson-Smith, et al.
Lancet (London, England)|July 28, 1979
Severe combined immune-deficiency disease in patient with alpha 1-antitrypsin deficiencyE W Gelfand, D W Cox, M T Lin, et al.
American Journal of Human Genetics|May 1, 1995
Wilson disease in Iceland: a clinical and genetic studyG R Thomas, O Jensson, G Gudmundsson, et al.
Human Molecular Genetics|January 1, 1993
Polymorphism of the protein C inhibitor (PCI) gene on chromosome 14K J Ashbourne, B C Byth, J C Meijers, et al.
Human Mutation|August 10, 2005
Twenty-four novel mutations in Wilson disease patients of predominantly European ancestryD W Cox, L Prat, J M Walshe, et al.
Genomics|August 10, 1995
Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8V Reed, P Williamson, P C Bull, et al.
American Journal of Human Genetics|June 1, 1989
In-frame single codon deletion in the Mmalton deficiency allele of alpha 1-antitrypsinG C Fraizer, T R Harrold, M H Hofker, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1983
Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locusP S Linsley, N T Bech-Hansen, L Siminovitch, et al.
Pageof 23