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P Scambler

Showing results (11-20 of 58) with videos related to

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Journal of Medical Genetics|October 1, 1993
DiGeorge syndrome: part of CATCH 22D I Wilson, J Burn, P Scambler, et al.
Oncogene|August 5, 1998
Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumourR G Grundy, J Pritchard, P Scambler, et al.
Journal of Biomechanics|July 20, 2011
Fluid-structure interaction study of the edge-to-edge repair technique on the mitral valveK D Lau, V Díaz-Zuccarini, P Scambler, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Linkage between the cystic fibrosis locus and markers on chromosome 7qB Wainwright, P Scambler, M Farrall, et al.
British Journal of Cancer|November 20, 1998
Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumourR G Grundy, J Pritchard, P Scambler, et al.
American Journal of Human Genetics|June 1, 1997
Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical regionH O'Donnell, C McKeown, C Gould, et al.
American Journal of Human Genetics|May 20, 1999
Evidence for the genetic heterogeneity of nephropathic phenotypes associated with Denys-Drash and Frasier syndromesA B Koziell, R Grundy, T M Barratt, et al.
Mechanisms of Development|December 4, 2001
Cloning of HOXD1 from unfertilised human oocytes and expression analyses during murine oogenesis and embryogenesisJ E Pitera, P J Milla, P Scambler, et al.
Molecular and Cellular Biology|July 22, 1998
RhoE regulates actin cytoskeleton organization and cell migrationR M Guasch, P Scambler, G E Jones, et al.
Biochemical and Biophysical Research Communications|August 26, 1998
Cloning, chromosome mapping and expression analysis of the HIRA gene from Drosophila melanogasterR Llevadot, G Marqués, M Pritchard, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|October 1, 1993
DiGeorge syndrome: part of CATCH 22D I Wilson, J Burn, P Scambler, et al.
Oncogene|August 5, 1998
Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumourR G Grundy, J Pritchard, P Scambler, et al.
Journal of Biomechanics|July 20, 2011
Fluid-structure interaction study of the edge-to-edge repair technique on the mitral valveK D Lau, V Díaz-Zuccarini, P Scambler, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Linkage between the cystic fibrosis locus and markers on chromosome 7qB Wainwright, P Scambler, M Farrall, et al.
British Journal of Cancer|November 20, 1998
Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumourR G Grundy, J Pritchard, P Scambler, et al.
American Journal of Human Genetics|June 1, 1997
Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical regionH O'Donnell, C McKeown, C Gould, et al.
American Journal of Human Genetics|May 20, 1999
Evidence for the genetic heterogeneity of nephropathic phenotypes associated with Denys-Drash and Frasier syndromesA B Koziell, R Grundy, T M Barratt, et al.
Mechanisms of Development|December 4, 2001
Cloning of HOXD1 from unfertilised human oocytes and expression analyses during murine oogenesis and embryogenesisJ E Pitera, P J Milla, P Scambler, et al.
Molecular and Cellular Biology|July 22, 1998
RhoE regulates actin cytoskeleton organization and cell migrationR M Guasch, P Scambler, G E Jones, et al.
Biochemical and Biophysical Research Communications|August 26, 1998
Cloning, chromosome mapping and expression analysis of the HIRA gene from Drosophila melanogasterR Llevadot, G Marqués, M Pritchard, et al.
Pageof 6