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P Scambler

Showing results (31-40 of 58) with videos related to

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Journal of Medical Genetics|August 1, 1986
Cystic fibrosis carrier detection using a linked gene probeM Farrall, P Scambler, K W Klinger, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1996
Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegansP Rizzu, E A Lindsay, C Taylor, et al.
Journal of Medical Genetics|October 1, 1993
Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11J Burn, A Takao, D Wilson, et al.
Cell|January 25, 1991
A new nomenclature for int-1 and related genes: the Wnt gene familyR Nusse, A Brown, J Papkoff, et al.
Cytogenetics and Cell Genetics|January 1, 1987
A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markersB Wainwright, N Lench, K Davies, et al.
American Journal of Human Genetics|November 1, 1987
Exclusion of catalytic and regulatory subunits of cAMP-dependent protein kinase as candidate genes for the defect causing cystic fibrosisP Scambler, O Oyen, B Wainwright, et al.
Somatic Cell and Molecular Genetics|November 1, 1989
Molecular cloning and localization to chromosome 6 of mouse INT1L1 geneA M Chan, J Hilkens, V Kroezen, et al.
Science (New York, N.Y.)|December 4, 1987
The gene for familial polyposis coli maps to the long arm of chromosome 5M Leppert, M Dobbs, P Scambler, et al.
Circulation Research|February 5, 1999
HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septationM J Farrell, H Stadt, K T Wallis, et al.
European Journal of Pediatrics|November 1, 1994
Clinical and molecular study of DiGeorge sequenceA Levy-Mozziconacci, F Wernert, P Scambler, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|August 1, 1986
Cystic fibrosis carrier detection using a linked gene probeM Farrall, P Scambler, K W Klinger, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1996
Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegansP Rizzu, E A Lindsay, C Taylor, et al.
Journal of Medical Genetics|October 1, 1993
Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11J Burn, A Takao, D Wilson, et al.
Cell|January 25, 1991
A new nomenclature for int-1 and related genes: the Wnt gene familyR Nusse, A Brown, J Papkoff, et al.
Cytogenetics and Cell Genetics|January 1, 1987
A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markersB Wainwright, N Lench, K Davies, et al.
American Journal of Human Genetics|November 1, 1987
Exclusion of catalytic and regulatory subunits of cAMP-dependent protein kinase as candidate genes for the defect causing cystic fibrosisP Scambler, O Oyen, B Wainwright, et al.
Somatic Cell and Molecular Genetics|November 1, 1989
Molecular cloning and localization to chromosome 6 of mouse INT1L1 geneA M Chan, J Hilkens, V Kroezen, et al.
Science (New York, N.Y.)|December 4, 1987
The gene for familial polyposis coli maps to the long arm of chromosome 5M Leppert, M Dobbs, P Scambler, et al.
Circulation Research|February 5, 1999
HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septationM J Farrell, H Stadt, K T Wallis, et al.
European Journal of Pediatrics|November 1, 1994
Clinical and molecular study of DiGeorge sequenceA Levy-Mozziconacci, F Wernert, P Scambler, et al.
Pageof 6