Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

Por Maher, E R, Webster, A R, Richards, F M, Green, J S, Crossey, P A, Payne, S J, Moore, A T
Publicado em 1996

Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma.

Por Crossey, P A, Eng, C, Ginalska-Malinowska, M, Lennard, T W, Wheeler, D C, Ponder, B A, Maher, E R
Publicado em 1995

Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene.

Por Richards, F M, Maher, E R, Latif, F, Phipps, M E, Tory, K, Lush, M, Crossey, P A, Oostra, B, Enblad, P, Gustavson, K H
Publicado em 1993

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.

Por Eng, C, Crossey, P A, Mulligan, L M, Healey, C S, Houghton, C, Prowse, A, Chew, S L, Dahia, P L, O'Riordan, J L, Toledo, S P
Publicado em 1995

Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22.

Por Foster, K., Crossey, P. A., Cairns, P., Hetherington, J. W., Richards, F. M., Jones, M. H., Bentley, E., Affara, N. A., Ferguson-Smith, M. A., Maher, E. R.
Publicado em 1994