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Showing results (41-50 of 58) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|December 11, 1991
Toward an animal model of cystic fibrosis: targeted interruption of exon 10 of the cystic fibrosis transmembrane regulator gene in embryonic stem cellsB H Koller, H S Kim, A M Latour, et al.
Genome Research|October 6, 1999
Duplications on human chromosome 22 reveal a novel Ret Finger Protein-like gene family with sense and endogenous antisense transcriptsE Seroussi, D Kedra, H Q Pan, et al.
American Journal of Human Genetics|June 1, 1995
Molecular definition of the 22q11 deletions in velo-cardio-facial syndromeB Morrow, R Goldberg, C Carlson, et al.
Nucleic Acids Research|November 11, 1986
Genetic homogeneity of cystic fibrosisK Klinger, P Stanislovitis, N Hoffman, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3)B Dechairo, C Dimon, D van Heel, et al.
Nature Genetics|August 1, 1996
A common region of 10p deleted in DiGeorge and velocardiofacial syndromesS C Daw, C Taylor, M Kraman, et al.
Lancet (London, England)|June 21, 1986
First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probesM Farrall, H Y Law, C H Rodeck, et al.
Clinical Genetics|June 11, 1999
Partial DiGeorge syndrome in two patients with a 10p rearrangementH Van Esch, P Groenen, S Daw, et al.
Human Genetics|January 1, 1985
Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19J A Donald, S C Wallis, A Kessling, et al.
Nature|August 13, 1987
Localization of the gene for familial adenomatous polyposis on chromosome 5W F Bodmer, C J Bailey, J Bodmer, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Proceedings of the National Academy of Sciences of the United States of America|December 11, 1991
Toward an animal model of cystic fibrosis: targeted interruption of exon 10 of the cystic fibrosis transmembrane regulator gene in embryonic stem cellsB H Koller, H S Kim, A M Latour, et al.
Genome Research|October 6, 1999
Duplications on human chromosome 22 reveal a novel Ret Finger Protein-like gene family with sense and endogenous antisense transcriptsE Seroussi, D Kedra, H Q Pan, et al.
American Journal of Human Genetics|June 1, 1995
Molecular definition of the 22q11 deletions in velo-cardio-facial syndromeB Morrow, R Goldberg, C Carlson, et al.
Nucleic Acids Research|November 11, 1986
Genetic homogeneity of cystic fibrosisK Klinger, P Stanislovitis, N Hoffman, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3)B Dechairo, C Dimon, D van Heel, et al.
Nature Genetics|August 1, 1996
A common region of 10p deleted in DiGeorge and velocardiofacial syndromesS C Daw, C Taylor, M Kraman, et al.
Lancet (London, England)|June 21, 1986
First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probesM Farrall, H Y Law, C H Rodeck, et al.
Clinical Genetics|June 11, 1999
Partial DiGeorge syndrome in two patients with a 10p rearrangementH Van Esch, P Groenen, S Daw, et al.
Human Genetics|January 1, 1985
Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19J A Donald, S C Wallis, A Kessling, et al.
Nature|August 13, 1987
Localization of the gene for familial adenomatous polyposis on chromosome 5W F Bodmer, C J Bailey, J Bodmer, et al.
Pageof 6