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Publications by P S Harper

Absence of Close Linkage Between Benign Hereditary Chorea and the Locus D4S10 (Probe G8).

Journal of Medical Genetics

English

What Do We Mean by Genetic Testing?

Journal of Medical Genetics

English

Molecular Genetics of Neurofibromatosis Type 1 (NF1).

Journal of Medical Genetics

English

Charcot-Marie-Tooth Disease Type 1a (CMT1a): Evidence for Trisomy of the Region P11.2 of Chromosome 17 in South Wales Families.

Journal of Medical Genetics

English

Minimal Expression of Myotonic Dystrophy: A Clinical and Molecular Analysis.

Journal of Medical Genetics

English

Genetics Services in the Community.

Journal of Medical Genetics

English

An Unusual Form of Familial Acrocephalosyndactyly.

Journal of Medical Genetics

English

The Natural History of Congenital Myotonic Dystrophy: Mortality and Long Term Clinical Aspects.

Archives of Disease in Childhood

English

Application of a Closely Linked Polymorphism of Restriction Fragment Length to Counselling and Prenatal Testing in Families With Myotonic Dystrophy.

English