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

C G Mathew

Showing results (91-100 of 129) with videos related to

Pageof 13
Sort By:
Journal of Medical Genetics|June 1, 1985
Polymorphism of DNA sequence in the human pro alpha 2(I) collagen geneA F Grobler-Rabie, D K Brebner, S Vandenplas, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal prediction of spinal muscular atrophyR J Daniels, G K Suthers, K E Morrison, et al.
American Journal of Human Genetics|January 1, 1989
Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type IC G Mathew, K Thorpe, D F Easton, et al.
American Journal of Human Genetics|August 11, 2000
Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group AH Joenje, M Levitus, Q Waisfisz, et al.
Nature|August 6, 1987
A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10C G Mathew, K S Chin, D F Easton, et al.
Journal of Gastroenterology and Hepatology|March 27, 2015
Defective macrophage handling of Escherichia coli in Crohn's diseaseT R Elliott, B N Hudspith, N B Rayment, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|July 20, 1991
Multiple endocrine neoplasia type 2A (MEN 2A) syndrome in a South African family. Biochemistry and molecular geneticsS Jansen, C G Mathew, W J Vermaak, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2001
Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South AfricaA J Tipping, T Pearson, N V Morgan, et al.
Genomics|March 1, 1990
The CEPH consortium primary linkage map of human chromosome 10R L White, J M Lalouel, Y Nakamura, et al.
Gut|January 13, 2001
Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel diseaseJ Hampe, N J Lynch, S Daniels, et al.
Pageof 13

Showing results (91-100 of 129) with videos related to

Sort By:
Pageof 13
Journal of Medical Genetics|June 1, 1985
Polymorphism of DNA sequence in the human pro alpha 2(I) collagen geneA F Grobler-Rabie, D K Brebner, S Vandenplas, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal prediction of spinal muscular atrophyR J Daniels, G K Suthers, K E Morrison, et al.
American Journal of Human Genetics|January 1, 1989
Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type IC G Mathew, K Thorpe, D F Easton, et al.
American Journal of Human Genetics|August 11, 2000
Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group AH Joenje, M Levitus, Q Waisfisz, et al.
Nature|August 6, 1987
A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10C G Mathew, K S Chin, D F Easton, et al.
Journal of Gastroenterology and Hepatology|March 27, 2015
Defective macrophage handling of Escherichia coli in Crohn's diseaseT R Elliott, B N Hudspith, N B Rayment, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|July 20, 1991
Multiple endocrine neoplasia type 2A (MEN 2A) syndrome in a South African family. Biochemistry and molecular geneticsS Jansen, C G Mathew, W J Vermaak, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2001
Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South AfricaA J Tipping, T Pearson, N V Morgan, et al.
Genomics|March 1, 1990
The CEPH consortium primary linkage map of human chromosome 10R L White, J M Lalouel, Y Nakamura, et al.
Gut|January 13, 2001
Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel diseaseJ Hampe, N J Lynch, S Daniels, et al.
Pageof 13