PhillipFullwoodMD

PubMed

• Frequent 3p allele loss and epigenetic inactivation of the RASSF1A tumour suppressor gene from region 3p21.3 in head and neck squamous cell carcinoma.
  Hogg, R. P., Honorio, S., Martinez, A., Agathanggelou, A., Dallol, A., Fullwood, P., Weichselbaum, R., Kuo, M. J., Maher, E. R., Latif, F.> ;Eur J Cancer. 2002 Aug
• Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours.
  Agathanggelou, A., Honorio, S., Macartney, D. P., Martinez, A., Dallol, A., Rader, J., Fullwood, P., Chauhan, A., Walker, R., Shaw, J. A., Hosoe, S., Lerman, M. I., Mi...> ;Oncogene. 2001 Mar 22
• Role of chromosome 3p12-p21 tumour suppressor genes in clear cell renal cell carcinoma: analysis of VHL dependent and VHL independent pathways of tumorigenesis.
  Martinez, A., Fullwood, P., Kondo, K., Kishida, T., Yao, M., Maher, E. R., Latif, F.> ;MP, Mol Pathol. 2000 Jun
• Detailed genetic and physical mapping of tumor suppressor loci on chromosome 3p in ovarian cancer.
  Fullwood, P., Marchini, S., Rader, J. S., Martinez, A., Macartney, D., Broggini, M., Morelli, C., Barbanti-Brodano, G., Maher, E. R., Latif, F.> ;Cancer Res. 1999 Sep 15
• No evidence for uniparental disomy as a common cause of Sotos syndrome.
  Smith, M., Fullwood, P., Qi, Y., Palmer, S., Upadhyaya, M., Cole, T.> ;J Med Genet. 1997 Jan
• X linked exudative vitreoretinopathy: clinical features and genetic linkage analysis.
  Fullwood, P., Jones, J., Bundey, S., Dudgeon, J., Fielder, A. R., Kilpatrick, M. W.> ;Br J Ophthalmol. 1993 Mar
• Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.
  Glass, I. A., Good, P., Coleman, M. P., Fullwood, P., Giles, M. G., Lindsay, S., Nemeth, A. H., Davies, K. E., Willshaw, H. A., Fielder, A.> ;J Med Genet. 1993 Dec
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