P S Harper

An integrated microcomputer system to maintain a genetic register for Huntington disease.

M Sarfarazi, O W Quarrell, G Wolak, 1987, American journal of medical genetics.

Population based study of late onset cerebellar ataxia in south east Wales

D Ravine, P S Harper, C. Wiles, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain.

P S Harper, P. Harper, P. Lowenstein, 1996, Human molecular genetics.

Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.

P S Harper, D Curtis, S. Folstein, 1996, American journal of human genetics.

Molecular genetics of neurofibromatosis type 1 (NF1).

P S Harper, P. Harper, M. Upadhyaya, 1996, Journal of medical genetics.