Table of contents

Research Article

• Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy. (1 December, 1978)

  J Pearn
• Genetic studies of acute infantile spinal muscular atrophy (SMA type I). An analysis of sex ratios, segregation ratios, and sex influence. (1 December, 1978)

  J Pearn
• Segregation analysis of chronic childhood spinal muscular atrophy. (1 December, 1978)

  J Pearn
• Genetics of adolescent idiopathic scoliosis. (1 December, 1978)

  A Czeizel, A Bellyei, O Barta, T Magda, L Molnár
• Angiokeratoma corporis diffusum (Anderson-Fabry disease) in a single large family in Nova Scotia. (1 December, 1978)

  M W Spence, J T Clarke, D M D'Entremont, G A Sapp, E R Smith, A L Goldbloom, G Davar
• A report on genetic registers. Based on the report of the Clinical Genetics Society Working Party. (1 December, 1978)

  A E Emery, C Brough, M Crawfurd, P Harper, R Harris, G Oakshott
• Thalassaemia types and their incidence in Sardinia. (1 December, 1978)

  A Cao, R Galanello, M Furbetta, P P Muroni, L Garbato, C Rosatelli, M T Scalas, M Addis, R Ruggeri, L Maccioni, M A Melis
• Thalassaemia of intermediate severity resulting from the interaction between alpha- and beta-thalassaemia. (1 December, 1978)

  S Musumeci, G Schilirò, G Pizzarelli, A Fischer, G Russo
• Taurodontism and Klinefelter's syndrome. (1 December, 1978)

  Y Komatz, T Tomoyoshi, O Yoshida, A Fujimoto, K Yoshitake
• Report of a mucopolysaccharidosis occurring in Australian aborigines. (1 December, 1978)

  H R Taylor, F C Hollows, J J Hopwood, E F Robertson
• Meckel syndrome and the prenatal diagnosis of neural tube defects. (1 December, 1978)

  M J Seller
• X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies. (1 December, 1978)

  R Bernstein, J Wagner, J Isdale, G T Nurse, A B Lane, T Jenkins
• Prenatal diagnosis of a de novo Y/22 translocation. (1 December, 1978)

  M Verjaal, P E Treffers, Y Nagal, N J Leschot
• Partial trisomy 6p with karyotype 46,XY,der(22), t(6;22)(p22;q13)mat. (1 December, 1978)

  G B Côté, S Papadakou-Lagoyanni, S Sbyrakis
• Osteosarcoma in a patient with Hutchinson-Gilford progeria. (1 December, 1978)

  C R King, J Lemmer, J R Campbell, A R Atkins
• The Aase syndrome in a female infant. (1 December, 1978)

  M C Higginbottom, K L Jones, F H Kung, T K Koch, J L Boyer
• Predisposition to spina bifida. (1 December, 1978)

  P A Stanway, I M Samloff, C J Brace, J H Renwick, C J Schorah
• A 'new' syndrome of mental retardation with characteristic facies and brachyphalangy. (1 December, 1978)

  G Turner
• Supernumerary small ring chromosome. (1 December, 1978)

  M S Lungarotti, A Calabro