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P Goodfellow

Showing results (61-70 of 68) with videos related to

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Nature|March 24, 1983
Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosomeP Goodfellow, G Banting, D Sheer, et al.
Gastroenterology|October 19, 2001
The interleukin 1 receptor antagonist gene allele 2 as a predictor of pouchitis following colectomy and IPAA in ulcerative colitisM J Carter, F S Di Giovine, A Cox, et al.
American Journal of Human Genetics|January 1, 1991
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)F Rousseau, A Vincent, S Rivella, et al.
Genomics|July 1, 1996
Physical mapping of the bloom syndrome region by the identification of YAC and P1 clones from human chromosome 15 band q26.1J Straughen, S Ciocci, T Z Ye, et al.
The New England Journal of Medicine|October 18, 1984
Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosomeC J Curry, R E Magenis, M Brown, et al.
Transplantation Proceedings|March 1, 1977
Serologic characterization of human Ia antigens using B-cell lymphoid linesJ Bodmer, D Young, E Jones, et al.
Brain : a Journal of Neurology|November 3, 1998
The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screenJ Chataway, R Feakes, F Coraddu, et al.
Human Molecular Genetics|July 1, 1993
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTCH Donis-Keller, S Dou, D Chi, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Nature|March 24, 1983
Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosomeP Goodfellow, G Banting, D Sheer, et al.
Gastroenterology|October 19, 2001
The interleukin 1 receptor antagonist gene allele 2 as a predictor of pouchitis following colectomy and IPAA in ulcerative colitisM J Carter, F S Di Giovine, A Cox, et al.
American Journal of Human Genetics|January 1, 1991
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)F Rousseau, A Vincent, S Rivella, et al.
Genomics|July 1, 1996
Physical mapping of the bloom syndrome region by the identification of YAC and P1 clones from human chromosome 15 band q26.1J Straughen, S Ciocci, T Z Ye, et al.
The New England Journal of Medicine|October 18, 1984
Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosomeC J Curry, R E Magenis, M Brown, et al.
Transplantation Proceedings|March 1, 1977
Serologic characterization of human Ia antigens using B-cell lymphoid linesJ Bodmer, D Young, E Jones, et al.
Brain : a Journal of Neurology|November 3, 1998
The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screenJ Chataway, R Feakes, F Coraddu, et al.
Human Molecular Genetics|July 1, 1993
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTCH Donis-Keller, S Dou, D Chi, et al.
Pageof 7