S. Cochrane

A previously undescribed mutation within the tetramerisation domain of TP53 in a family with Li-Fraumeni syndrome.

D. Evans, J. Varley, J. Boyle, 1996, Oncogene.

An evaluation of common breast cancer gene mutations in a population of Ashkenazi Jews.

A. Howell, D. Evans, J. Varley, 1998, Journal of medical genetics.

Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)

A. Monaco, S. Cochrane, N. Haites, 1994, Human molecular genetics.

Jews . mutations in a population of Ashkenazi An evaluation of common breast cancer gene

A. Howell, J. Varley, S. Cochrane, 2022 .

Serum soluble CD23 in patients with hypogammaglobulinaemia

S. Cochrane, P. Wilson, A. Bansal, 1994, Clinical and experimental immunology.

X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms.

A. Monaco, K. Fischbeck, S. Cochrane, 1994, Journal of medical genetics.

Surveillance of adverse reactions in patients self-infusing intravenous immunoglobulin at home

C. Fletcher, S. Cochrane, V. Brennan, 1995, Journal of Clinical Immunology.

Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration.

J. J. Shepherd, D. Sillence, L. Mestroni, 1994, Journal of medical genetics.