Table of contents

Research Article

• Medical genetics in China: a western view. (1 October, 1986)

  P S Harper, R Harris
• Williams syndrome. (1 October, 1986)

  J Burn
• The frequency of the fragile X chromosome among schoolchildren in Coventry. (1 October, 1986)

  T P Webb, S Bundey, A Thake, J Todd
• Twelve families with fragile X(q27). (1 October, 1986)

  T Webb, A Thake, J Todd
• Replication status of fragile X(q27.3) in 13 female heterozygotes. (1 October, 1986)

  E Tuckerman, T Webb, A Thake
• Mutations linked to the pro alpha 2(I) collagen gene are responsible for several cases of osteogenesis imperfecta type I. (1 October, 1986)

  G Wallis, P Beighton, C Boyd, C G Mathew
• A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19. (1 October, 1986)

  B Wainwright, M Farrall, E Watson, R Williamson
• A new strategy for mapping the human genome. (1 October, 1986)

  D J Shaw
• Pseudoachondroplasia: clinical diagnosis at different ages and comparison of autosomal dominant and recessive types. A review of 32 patients (26 kindreds). (1 October, 1986)

  R Wynne-Davies, C M Hall, I D Young
• Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2). (1 October, 1986)

  J Brusnický, K M van Heerden, G de Jong, A S Cronjé, A E Retief
• Segregation of a t(3;20) translocation through three generations resulting in unbalanced karyotypes in six persons. (1 October, 1986)

  K B Nielsen, N Tommerup, B Jespersen, P Nygaard, L Kleif
• The effects of severe mixed environmental pollution on human chromosomes. (1 October, 1986)

  A Katsantoni, S Nakou, I Antoniadou-Koumatou, G B Côté
• Pitfalls in prenatal diagnosis of beta thalassaemia. (1 October, 1986)

  C Rosatelli, L Maccioni, M T Scalas, A Cao
• Microtia with meatal atresia and conductive deafness: mild and severe manifestations within the same sibship. (1 October, 1986)

  P Strisciuglio, A Ballabio, G Parenti
• Partial trisomy 7 (q32----qter) syndrome in two children. (1 October, 1986)

  D A Couzin, N Haites, J L Watt, A W Johnston
• Three children with partial trisomy 1q and partial monosomy 3p. (1 October, 1986)

  G T McCarthy, C N Fear, A C Berry
• A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome. (1 October, 1986)

  R D Jefferson, J Burn, K L Gaunt, S Hunter, E V Davison
• A de novo X;13 translocation with abnormal phenotype. (1 October, 1986)

  S V Hodgson, J C Barber, A Dowie, V Dubowitz
• Terminal deletion of the long arm of chromosome 10. (1 October, 1986)

  H Curtis, R T Howell, C Cope