Table of contents

Research Article

• Hereditary fructose intolerance. (1 May, 1998)

  M Ali, P Rellos, T M Cox
• A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK. (1 May, 1998)

  A C Hutchesson, S Bundey, M A Preece, S K Hall, A Green
• Prediction of liability to orofacial clefting using genetic and craniofacial data from parents. (1 May, 1998)

  P A Mossey, R Arngrimsson, J McColl, G M Vintiner, J M Connor
• Abnormalities of dystrophin, the sarcoglycans, and laminin alpha2 in the muscular dystrophies. (1 May, 1998)

  K J Jones, S S Kim, K N North
• Molecular study of the rhodopsin gene in retinitis pigmentosa patients in the Basque Country. (1 May, 1998)

  A I Alvarez, E Arostegui, R Martin, M Duran, M L Onaindia, M Molina, M I Tejada
• Linkage analysis in Usher syndrome type I (USH1) families from Spain. (1 May, 1998)

  C Espinós, C Nájera, J M Millán, C Ayuso, M Baiget, H Pérez-Garrigues, O Rodrigo, C Vilela, M Beneyto
• Genotype-phenotype correlation in L1 associated diseases. (1 May, 1998)

  E Fransen, G Van Camp, R D'Hooge, L Vits, P J Willems
• Psychosocial adaptation in adolescents and young adults with Marfan syndrome: an exploratory study. (1 May, 1998)

  A Van Tongerloo, A De Paepe
• Recommendations for education and training of genetic nurses and counsellors in the United Kingdom. (1 May, 1998)

  H Skirton, C Barnes, P Guilbert, A Kershaw, L Kerzin-Storrar, C Patch, G Curtis, J Walford-Moore
• The North Cumbria Community Genetics Project. (1 May, 1998)

  D S Chase, E J Tawn, L Parker, P Jonas, C O Parker, J Burn
• Autosomal dominant juvenile recurrent parotitis. (1 May, 1998)

  E Reid, F Douglas, Y Crow, A Hollman, J Gibson
• 49,XXXXY: a distinct phenotype. Three new cases and review. (1 May, 1998)

  J Peet, D D Weaver, G H Vance
• Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay. (1 May, 1998)

  F L Long, D P Duckett, L J Billam, D K Williams, J A Crolla
• A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q. (1 May, 1998)

  M Papaioannou, D Bessant, A Payne, J Bellingham, C Rougas, A Loutradis-Anagnostou, C Gregory-Evans, A Balassopoulou, S Bhattacharya
• Exclusion of the familial Mediterranean fever locus as a susceptibility region for autosomal dominant familial Hibernian fever. (1 May, 1998)

  M F McDermott, E M McDermott, K A Quane, L C Jones, B W Ogunkolade, D Curtis, F Waldron-Lynch, M Phelan, G A Hitman, M G Molloy, R J Powell
• Unknown syndrome: peculiar face, severe hypodontia of permanent teeth, and precocious choroid calcifications. (1 May, 1998)

  R Pallotta, P Fusilli