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J K Cowell

Showing results (41-50 of 131) with videos related to

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British Journal of Cancer|November 1, 1993
Mechanisms of oncogenesis in patients with familial retinoblastomaZ Onadim, A Hogg, J K Cowell
Human Molecular Genetics|June 9, 1998
NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastomaT Roberts, O Chernova, J K Cowell
Archives of Disease in Childhood|January 1, 1987
The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletionsJ K Cowell, E Thompson, P Rutland
Cancer Genetics and Cytogenetics|December 24, 1997
Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)T Roberts, O Chernova, J K Cowell
Genomics|September 1, 1996
Regional localization of 192 genic markers on human chromosome 1T Roberts, C Auffray, J K Cowell
European Journal of Human Genetics : EJHG|January 1, 1994
Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastomaJ K Cowell, T Smith, B Bia
Cancer Genetics and Cytogenetics|September 1, 1988
Cytogenetic changes in Wilms' tumorsV Solis, J Pritchard, J K Cowell
British Journal of Cancer|June 1, 1993
Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 geneJ K Cowell, N Groves, P Baird
Oncogene|January 18, 1996
A novel mutation in the promotor region in a family with a mild form of retinoblastoma indicates the location of a new regulatory domain for the RB1 geneJ K Cowell, B Bia, A Akoulitchev
Genomics|January 25, 2000
Identification of a novel gene (ADPRTL1) encoding a potential Poly(ADP-ribosyl)transferase proteinI H Still, P Vince, J K Cowell
Pageof 14

Showing results (41-50 of 131) with videos related to

Sort By:
Pageof 14
British Journal of Cancer|November 1, 1993
Mechanisms of oncogenesis in patients with familial retinoblastomaZ Onadim, A Hogg, J K Cowell
Human Molecular Genetics|June 9, 1998
NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastomaT Roberts, O Chernova, J K Cowell
Archives of Disease in Childhood|January 1, 1987
The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletionsJ K Cowell, E Thompson, P Rutland
Cancer Genetics and Cytogenetics|December 24, 1997
Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)T Roberts, O Chernova, J K Cowell
Genomics|September 1, 1996
Regional localization of 192 genic markers on human chromosome 1T Roberts, C Auffray, J K Cowell
European Journal of Human Genetics : EJHG|January 1, 1994
Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastomaJ K Cowell, T Smith, B Bia
Cancer Genetics and Cytogenetics|September 1, 1988
Cytogenetic changes in Wilms' tumorsV Solis, J Pritchard, J K Cowell
British Journal of Cancer|June 1, 1993
Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 geneJ K Cowell, N Groves, P Baird
Oncogene|January 18, 1996
A novel mutation in the promotor region in a family with a mild form of retinoblastoma indicates the location of a new regulatory domain for the RB1 geneJ K Cowell, B Bia, A Akoulitchev
Genomics|January 25, 2000
Identification of a novel gene (ADPRTL1) encoding a potential Poly(ADP-ribosyl)transferase proteinI H Still, P Vince, J K Cowell
Pageof 14