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Human Genetics|December 1, 1992
A single base pair polymorphism in the WT1 gene detected by single-strand conformation polymorphism analysisN Groves, P N Baird, A Hogg, et al.Oncogene|July 1, 1992
Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencingA Hogg, Z Onadim, P N Baird, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1992
Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotypeZ Onadim, A Hogg, P N Baird, et al.Human Molecular Genetics|August 1, 1992
Constitutional mutations in the WT1 gene in patients with Denys-Drash syndromeP N Baird, A Santos, N Groves, et al.Oncogene|November 1, 1992
Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndromeP N Baird, N Groves, D A Haber, et al.British Journal of Cancer|June 1, 1994
Molecular genetic analysis of chromosome 11p in familial Wilms tumourP N Baird, J Pritchard, J K CowellBritish 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 BairdBritish Journal of Cancer|November 1, 1993
Mechanisms of oncogenesis in patients with familial retinoblastomaZ Onadim, A Hogg, J K CowellProceedings of the National Academy of Sciences of the United States of America|August 1, 1993
Molecular mechanisms of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastomaA Hogg, B Bia, Z Onadim, et al.Pageof 35