P.S. Harper

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)

Peter Lunt, Philip Jardine, Manuela C. Koch et al. · Human Molecular Genetics · 1995 · 208 citations

THE NATURAL HISTORY OF THE SEVERE FORM OF HUNTER'S SYNDROME: A STUDY BASED ON 52 CASES

I D Young, P.S. Harper · Developmental Medicine & Child Neurology · 1983 · 174 citations

Congenital myotonic dystrophy in Britain. I. Clinical aspects.

P.S. Harper · Archives of Disease in Childhood · 1975 · 171 citations · Full text

Developmental Anomaly, Rare Diseases, Mendelian Disorder +15

Genetic risks for children of women with myotonic dystrophy.

Manuela C. Koch, T. Grimm, H G Harley et al. · PubMed · 1991 · 145 citations

Mild form of Hunter's syndrome: clinical delineation based on 31 cases.

I D Young, P.S. Harper · Archives of Disease in Childhood · 1982 · 142 citations · Full text