5
results
for author:"Heathcott R."
in Literature Citations
| Sequential WT1 and CTNNB1 mutations and alterations of beta-catenin localisation in intralobar nephrogenic rests and associated Wilms tumours: two case studies. Fukuzawa R., Heathcott R.W., More H.E., Reeve A.E. J. Clin. Pathol. 60:1013-1016(2007) · Mapped (6) |
| The DNA sequence and analysis of human chromosome 6. Mungall A.J., Palmer S.A., Sims S.K., Edwards C.A., Ashurst J.L., Wilming L., Jones M.C., Horton R., Hunt S.E., Scott C.E. et al. Nature 425:805-811(2003) · UniProtKB (1,570) |
| A necropsy case of Denys-Drash syndrome with a WT1 mutation in exon 7. Fukuzawa R., Sakamoto J., Heathcott R.W., Hata J.I. J. Med. Genet. 39:e48-e48(2002) · Mapped (7) |
| A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X. Heathcott R.W., Morison I.M., Gubler M.C., Corbett R., Reeve A.E. Hum. Mutat. 19:462-462(2002) · Mapped (7) |
| The DNA sequence of human chromosome 22. Dunham I., Hunt A.R., Collins J.E., Bruskiewich R., Beare D.M., Clamp M., Smink L.J., Ainscough R., Almeida J.P., Babbage A.K. et al. |
