Research samples from families with genetic diseases : a proposed code of conductHARPER, P. S.BMJ. British medical journal (International ed.). 1993, Vol 306, Num 6889, pp 1391-1394, issn 0959-8146Article

Genetic counselling and prenatal diagnosisHARPER, P. S.British medical bulletin. 1983, Vol 39, Num 4, pp 302-309, issn 0007-1420Article

Presymptomatic testing for Huntington's disease : a world wide surveyHARPER, P. S.Journal of medical genetics. 1993, Vol 30, Num 12, pp 1020-1022, issn 0022-2593Article

DNA markers and Duchenne muscular dystrophyHARPER, P. S.Archives of disease in childhood. 1984, Vol 59, Num 3, pp 195-196, issn 0003-9888Article

New genes for old diseases : the molecular basis of myotonic dystrophy and Huntington's disease : The Lumbeian Lecture 1995HARPER, P. S.Journal of the Royal College of Physicians of London. 1996, Vol 30, Num 3, pp 221-231, issn 0035-8819Article

Huntington disease and the abuse of geneticsHARPER, P. S.American journal of human genetics. 1992, Vol 50, Num 3, pp 460-464, issn 0002-9297Article

The epidemiology of Huntington's diseaseHARPER, P. S.Human genetics. 1992, Vol 89, Num 4, pp 365-376, issn 0340-6717Article

Insurance and genetic testingHARPER, P. S.Lancet (British edition). 1993, Vol 341, Num 8839, pp 224-227, issn 0140-6736Article

Postoperative complications in myotonic dystrophyHARPER, P. S.Lancet (British edition). 1989, Vol 2, Num 8674, issn 0140-6736, 1269 [1 p.]Article

The genetics of muscular dystrophiesHARPER, P. S.Progress in medical genetics. 1985, Vol 6, pp 53-90, issn 0079-6441Article

What do we mean by genetic testing?HARPER, P. S.Journal of medical genetics. 1997, Vol 34, Num 9, pp 749-752, issn 0022-2593Article

Naming of syndromes and unethical activities : the case of Hallervorden and SpatzHARPER, P. S.Lancet (British edition). 1996, Vol 348, Num 9036, pp 1224-1225, issn 0140-6736Article

A regional register for inherited cancersLITTLER, M; HARPER, P. S.British medical journal (1857). 1989, Vol 298, Num 6689, pp 1689-1691, issn 0007-1447Article

Genetic prediction and family structure in Huntington's choreaHARPER, P. S; SARFARAZI, M.British medical journal (1857). 1985, Vol 290, Num 6486, pp 1929-1930, issn 0007-1447Article

Testing may be unhelpfulHARPER, P. S; CLARKE, A.BMJ. British medical journal (International ed.). 1995, Vol 310, Num 6983, pp 857-858, issn 0959-8146Article

Should we test children for adult genetics diseases ?HARPER, P. S; CLARKE, A.Lancet (British edition). 1990, Vol 335, Num 8699, pp 1205-1206, issn 0140-6736Article

Molecular genetics of neurofibromatosis type 1 (NF1)MING HONG SHEN; HARPER, P. S; UPADHYAYA, M et al.Journal of medical genetics. 1996, Vol 33, Num 1, pp 2-17, issn 0022-2593Article

Molecular diagnostic analysis for Huntington's disease : a prospective evaluationMACMILLAN, J. C; DAVIES, P; HARPER, P. S et al.Journal of neurology, neurosurgery and psychiatry. 1995, Vol 58, Num 4, pp 496-498, issn 0022-3050Article

Genetic counselling in facioscapulohumeral muscular dystrophyLUNT, P. W; HARPER, P. S.Journal of medical genetics. 1991, Vol 28, Num 10, pp 655-664, issn 0022-2593Article

Single-gene neurological disorders in South Wales : an epidemiological studyMACMILLAN, J. C; HARPER, P. S.Annals of neurology. 1991, Vol 30, Num 3, pp 411-414, issn 0364-5134Article

Implications of diagnostic delay in Duchenne muscular dystrophyO'BRIEN, T; SIBERT, J. R; HARPER, P. S et al.British medical journal (1857). 1983, Vol 287, Num 6399, pp 1106-1107, issn 0007-1447Article

Outlook for a clinically normal child in a sibship with congenital myotonic dystrophyÓBRIEN, T; NEWCOMBE, R. G; HARPER, P. S et al.The Journal of pediatrics. 1983, Vol 103, Num 5, pp 762-763, issn 0022-3476Article

Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weaknessMCENTAGART, M; DUNSTAN, M; BELL, C et al.Journal of neurology, neurosurgery and psychiatry. 2002, Vol 73, Num 6, pp 762-765, issn 0022-3050, 4 p.Article

Ten years of presymptomatic testing for Huntington's disease : the experience of the UK Huntington's Disease Prediction ConsortiumHARPER, P. S; LIM, C; CRAUFURD, D et al.Journal of medical genetics. 2000, Vol 37, Num 8, pp 567-571, issn 0022-2593Article

Huntingtin interacts with cystathionine β-synthaseBOUTELL, J. M; WOOD, J. D; HARPER, P. S et al.Human molecular genetics (Print). 1998, Vol 7, Num 3, pp 371-378, issn 0964-6906Article