4
results
for author:"Heathcott R.W."
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) |
| 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. |
