MYOTONIC DYSTROPHYHARPER PS.1979; MAJOR PROBL. NEUROL.; GBR; DA. 1979; VOL. 9; 343 P.; BIBL. DISSEM.Serial Issue

MENDELIAN INHERITANCE OR TRANSMISSIBLE AGENT. THE LESSON OF KURU AND THE AUSTRALIA ANTIGEN.HARPER PS.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 6; PP. 389-398; BIBL. 1 P. 1/2Article

PRE-SYMPTOMATIC DETECTION AND GENETIC COUNSELLING IN MYOTONIC DYSTROPHY = DETECTION PRESYMPTOMATIQUE ET CONSEIL GENETIQUE DANS LA DYSTROPHIE MYOTONIQUEHARPER PS.1973; CLIN. GENET.; DANM.; DA. 1973; VOL. 4; NO 2; PP. 134-140; BIBL. 11REF.Serial Issue

BENIGN HEREDITARY CHOREA. CLINICAL AND GENETIC ASPECTS.HARPER PS.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 1; PP. 85-95; BIBL. 10 REF.Article

GENETIC VARIATION IN WALES.HARPER PS.1976; J. R. COLL. PHYSICIANS LONDON; G.B.; DA. 1976; VOL. 10; NO 4; PP. 321-332; BIBL. 34 REF.Article

CONGENITAL MYOTONIC DYSTROPHY IN BRITAIN. I. CLINICAL ASPECTS. = LA DYSTROPHIE MYOTONIQUE CONGENITALE EN GRANDE-BRETAGNE. I. ASPECTS CLINIQUESHARPER PS.1975; ARCH. DIS. CHILDH.; G.B.; DA. 1975; VOL. 50; NO 7; PP. 505-513; BIBL. 21 REF.Article

CONGENITAL MYOTONIC DYSTROPHY IN BRITAIN. II. GENETIC BASIS = LA DYSTROPHIE MYOTONIQUE CONGENITALE EN GRANDE-BRETAGNE. II. BASES GENETIQUESHARPER PS.1975; ARCH. DIS. CHILDH.; G.B.; DA. 1975; VOL. 50; NO 7; PP. 514-521; BIBL. 33 REF.Article

EARLY-ONSET DYSTROPHIA MYOTONICA EVIDENCE SUPPORTING A MATERNAL ENVIRONMENTAL FACTOR = ATTAQUE PRECOCE DE DYSTROPHIE MYOTONIQUE SUPPORTANT DE FACON CERTAINE UN FACTEUR ENVIRONNANT MATERNELHARPER PS.1972; LANCET; G.B.; DA. 1972; NO 7767; PP. 53-55; BIBL. 12REF.Article

THE PRENATAL DIAGNOSIS OF METABOLIC DISORDERS = LE DIAGNOSTIC PRENATAL DES DESORDRES METABOLIQUESHARPER PS.1973; J. R. COLL. PHYSICIANS LONDON; G.B.; DA. 1973; VOL. 7; NO 3; PP. 251-258; BIBL. 1P.Article

ATTITUDES OF SUBJECTS AT RISK AND THEIR RELATIVES TOWARDS GENETIC COUNSELLING IN HUNTINGTONS CHOREATYLER A; HARPER PS.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 3; PP. 179-188; BIBL. 18 REF.Article

AN UNUSUAL FORM OF FAMILIAL ACROCEPHALOSYNDACTYLYYOUNG ID; HARPER PS.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 4; PP. 286-288; BIBL. 7 REF.Article

INCIDENCE OF HUNTER'S SYNDROMEYOUNG ID; HARPER PS.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 4; PP. 391-392; BIBL. 4 REF.Article

HEREDITARY DISTAL SPINAL MUSCULAR ATROPHY WITH VOCAL CORD PARALYSISYOUNG ID; HARPER PS.1980; J. NEUROL. NEUROSURG. PSYCHIATRY; GBR; DA. 1980; VOL. 43; NO 5; PP. 413-418; BIBL. 14 REF.Article

GENETIC STUDY OF WELSH GYPSICS.WILLIAMS EM; HARPER PS.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 3; PP. 172-176; BIBL. 17 REF.Article

MULTIPLE FORMS OF IDURONATE 2-SULPHATE SULPHATASE IN HUMAN TISSUES AND BODY FLUIDSARCHER IM; HARPER PS; WUSTEMAN FS et al.1982; BIOCHIMICA ET BIOPHYSICA ACTA; ISSN 0006-3002; NLD; DA. 1982; VOL. 708; NO 2; PP. 134-140; BIBL. 9 REF.Article

FACTORS INFLUENCING AGE AT ONSET AND DURATION OF SURVIVAL IN HUNTINGTON'S CHOREANEWCOMBE RG; WALKER DA; HARPER PS et al.1981; ANN. HUM. GENET.; ISSN 0003-4800; GBR; DA. 1981; VOL. 45; NO 4; PP. 387-396; BIBL. 11 REF.Article

AN IMPROVED ASSAY FOR IDURONATE 2-SULPHATE SULPHATASE IN SERUM AND ITS USE IN THE DETECTION OF CARRIERS OF THE HUNTER SYNDROMEARCHER IM; HARPER PS; WUSTEMAN FS et al.1981; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1981; VOL. 112; NO 1; PP. 107-112; BIBL. 9 REF.Article

SYNDROME OF ICHTHYOSIS, HEPATOSPLENOMEGALY AND CEREBELLAR DEGENERATION-STEROID SULPHATASE ACTIVITYDYKES PJ; MARKS R; HARPER PS et al.1980; BRIT. J. DERMATOL.; GBR; DA. 1980; VOL. 102; NO 3; PP. 353-354; BIBL. 2 REF.Article

GENETIC MARKERS IN WELSH GYPSIES.HARPER PS; WILLIAMS EM; SUNDERLAND E et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 3; PP. 177-182; BIBL. 32 REF.Article

OROCRANIODIGITAL (JUBERG-HAYWARD) SYNDROME WITH GROWTH HORMONE DEFICIENCYKINGSTON HM; HUGHES IA; HARPER PS et al.1982; ARCHIVES OF DISEASES IN CHILDHOOD; ISSN 0003-9888; USA; DA. 1982; VOL. 57; NO 10; PP. 790-792; BIBL. 6 REF.Article

IN VITRO STUDIES ON CALCIUM ACTIVATED PHOSPHATIDYLINOSITOL PHOSPHODIESTERASE OF ERYTHROCYTE GHOSTS FROM NORMAL INDIVIDUALS AND THOSE WITH MYOTONIC MUSCULAR DYSTROPHYMEREDITH AL; HARPER PS; BRADLEY DM et al.1982; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1982; VOL. 120; NO 2; PP. 201-206; BIBL. 16 REF.Article

FAMILY BREAK-DOWN AND STRESS IN HUNTINGTON'S CHOREATYLER A; HARPER PS; DAVIES K et al.1983; JOURNAL OF BIOSOCIAL SCIENCE; ISSN 0021-9320; GBR; DA. 1983; VOL. 15; NO 2; PP. 127-138; BIBL. 20 REF.Article

HUNTINGTON'S CHOREA IN SOUTH WALES: MUTATION, FERTILITY, AND GENETIC FITNESSWALKER DA; HARPER PS; NEW COMBE RG et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 1; PP. 12-17; BIBL. 18 REF.Article

HUTINGTON'S CHOREA. THE BASIS FOR LONG-TERM PREVENTIONHARPER PS; TYLER A; WALKER DA et al.1979; LANCET; GBR; DA. 1979; NO 8138; PP. 346-349; BIBL. 2 REF.Article

DETECTION OF FEMALE CARRIERS OF HUNTER'S SYNDROME: COMPARISON OF SERUM AND HAIR-ROOT ANALYSISARCHER IM; REES DW; OLADIMEJI A et al.1982; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; SUPPL. 1; PP. 15-16; BIBL. 2 REF.Article