M. Williams

HMSN and HNPP: Laboratory Service Provision in the South West of England‐Two Years' Experience

D. L. Stevens, P. Turnpenny, L. Tyfield, 1999, Annals of the New York Academy of Sciences.

Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)

P. Harper, M. Koch, M. Upadhyaya, 1995, Human molecular genetics.

Carrier screening for cystic fibrosis in primary care: evaluation of a project in South Wales The South Wales Cystic Fibrosis Carrier Screening Research Team

A. Clarke, P. Harper, J. Cheadle, 1997, Clinical genetics.

Phenotypic–genotypic correlation will assist genetic counseling in 4q35‐facioscapulohumeral muscular dystrophy

P. Harper, M. Upadhyaya, J. Maynard, 1995, Muscle & nerve. Supplement.