E. Bentley

发表

The identification of novel gene sequences of the human adult testis.

M. Jones, N. Affara, A. Pelmear, 1994, Genomics.

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

M. Ferguson-Smith, P. Cairns, M. Jones, 1994, British Journal of Cancer.

Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein

N. Prescott, P. Scambler, C. Roberts, 2003, Nature Genetics.

Cloning of the X-linked glycerol kinase deficiency gene and its identification by sequence comparison to the Bacillus subtilis homologue.

M. Leversha, G. Besley, N. Affara, 1993, Human molecular genetics.

Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs

Martin S. Taylor, P. Scambler, I. Jackson, 2005, Nature Genetics.

Molecular genetic investigations of the mechanism of tumourigenesis in von Hippel-Lindau disease: analysis of allele loss in VHL tumours

K. Tory, M. Lerman, B. Zbar, 2004, Human Genetics.

Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis.

M. Lerman, B. Zbar, M. Ferguson-Smith, 1991, Genomics.

Mapping of Von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis

D. Barton, M. Ferguson-Smith, M. Ponder, 1990, Journal of the Neurological Sciences.

Fine mapping of 39 ESTs on human chromosome 6p23-p25.

J. Ragoussis, E. Bentley, M. Olavesen, 1997, Genomics.

D5Ucl1 and Els1 are closely linked to W on mouse Chromosome 5 but lie distal to the W19H deletion

D. Stephenson, A. Gossler, J. Inglis, 1996, Mammalian Genome.

Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markers.

D. Barton, J. Yates, M. Chiano, 1992, Journal of medical genetics.