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P Scambler

Showing results (1-10 of 58) with videos related to

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Nature Genetics|May 1, 1994
Human haploinsufficiency--one for sorrow, two for joyE Fisher, P Scambler
Clinical Genetics|August 17, 2000
Cortical dysgenesis in 2 patients with chromosome 22q11 deletionL M Bird, P Scambler
American Journal of Human Genetics|January 1, 1986
The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4M Farrall, P Scambler, P North, et al.
Journal of Medical Genetics|September 1, 1995
Monozygotic twins with chromosome 22q11 deletion and discordant phenotypeJ Goodship, I Cross, P Scambler, et al.
Lancet (London, England)|November 28, 1992
Possible role for COMT in psychosis associated with velo-cardio-facial syndromeI Dunham, J Collins, R Wadey, et al.
Gene|April 3, 1998
Isolation and genomic characterization of the TUPLE1/HIRA gene of the pufferfish Fugu rubripesR Llevadot, X Estivill, P Scambler, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 1, 1996
Genomic organization of TUPLE1/HIRA: a gene implicated in DiGeorge syndromeR Llevadot, P Scambler, X Estivill, et al.
Nucleic Acids Research|February 25, 1989
Probe pJ1 [D7S402] detects a MspI RFLP on chromosome 7q31-32M Ramsay, H Sutherland, R Williamson, et al.
Medical Engineering & Physics|August 13, 2010
Mitral valve dynamics in structural and fluid-structure interaction modelsK D Lau, V Diaz, P Scambler, et al.
Genomics|February 10, 1995
Cloning and mapping of murine Nfe2l1J McKie, K Johnstone, M G Mattei, et al.
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 6
Nature Genetics|May 1, 1994
Human haploinsufficiency--one for sorrow, two for joyE Fisher, P Scambler
Clinical Genetics|August 17, 2000
Cortical dysgenesis in 2 patients with chromosome 22q11 deletionL M Bird, P Scambler
American Journal of Human Genetics|January 1, 1986
The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4M Farrall, P Scambler, P North, et al.
Journal of Medical Genetics|September 1, 1995
Monozygotic twins with chromosome 22q11 deletion and discordant phenotypeJ Goodship, I Cross, P Scambler, et al.
Lancet (London, England)|November 28, 1992
Possible role for COMT in psychosis associated with velo-cardio-facial syndromeI Dunham, J Collins, R Wadey, et al.
Gene|April 3, 1998
Isolation and genomic characterization of the TUPLE1/HIRA gene of the pufferfish Fugu rubripesR Llevadot, X Estivill, P Scambler, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 1, 1996
Genomic organization of TUPLE1/HIRA: a gene implicated in DiGeorge syndromeR Llevadot, P Scambler, X Estivill, et al.
Nucleic Acids Research|February 25, 1989
Probe pJ1 [D7S402] detects a MspI RFLP on chromosome 7q31-32M Ramsay, H Sutherland, R Williamson, et al.
Medical Engineering & Physics|August 13, 2010
Mitral valve dynamics in structural and fluid-structure interaction modelsK D Lau, V Diaz, P Scambler, et al.
Genomics|February 10, 1995
Cloning and mapping of murine Nfe2l1J McKie, K Johnstone, M G Mattei, et al.
Pageof 6