Tom Strachan

Germline mutations in the neurofibromatosis type 2 tumour suppressor gene.

T. Strachan, D. Bourn, D. Gareth, 1994, Human molecular genetics.

A disease-associated germline deletion maps the type 2 neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukaemia inhibitory factor locus.

L. Gaunt, T. Strachan, R. Harris, 1993, Human molecular genetics.

A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individuals.

D. Evans, T. Strachan, J. Goodship, 1994, American journal of human genetics.

Diagnostic issues in a family with late onset type 2 neurofibromatosis.

D. Evans, T. Strachan, R. Ramsden, 1995, Journal of medical genetics.

Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndrome.

I. Krantz, M. Devoto, M. Hofreiter, 2001, American journal of medical genetics.

Dynamics of concerted evolution of ribosomal DNA and histone gene families in the melanogaster species subgroup of Drosophila.

T. Strachan, E. Coen, G. Dover, 1982, Journal of molecular biology.