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Journal of Medical Genetics
|
October 1, 1993
DiGeorge syndrome: part of CATCH 22
D 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 tumour
R 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 valve
K 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 7q
B Wainwright, P Scambler, M Farrall, et al.
British Journal of Cancer
|
November 20, 1998
Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour
R 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 region
H 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 syndromes
A 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 embryogenesis
J E Pitera, P J Milla, P Scambler, et al.
Molecular and Cellular Biology
|
July 22, 1998
RhoE regulates actin cytoskeleton organization and cell migration
R 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 melanogaster
R Llevadot, G Marqués, M Pritchard, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 58) with videos related to
Sort By:
Page
of 6
Journal of Medical Genetics
|
October 1, 1993
DiGeorge syndrome: part of CATCH 22
D 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 tumour
R 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 valve
K 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 7q
B Wainwright, P Scambler, M Farrall, et al.
British Journal of Cancer
|
November 20, 1998
Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour
R 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 region
H 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 syndromes
A 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 embryogenesis
J E Pitera, P J Milla, P Scambler, et al.
Molecular and Cellular Biology
|
July 22, 1998
RhoE regulates actin cytoskeleton organization and cell migration
R 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 melanogaster
R Llevadot, G Marqués, M Pritchard, et al.
Page
of 6