Table of contents

Research Article

• Diaphragmatic hernia in the south-west of England. (1 August, 1976)

  T J David, C A Illingworth
• Congenital malformations associated with anencephaly and iniencephaly. (1 August, 1976)

  T J David, A Nixon
• Syndrome designations. (1 August, 1976)

  M M Cohen
• Probable common origin of a hereditary fundus dystrophy (Sorsby's familial pseudoinflammatory macular dystrophy) in an English and Australian family. (1 August, 1976)

  H Kalmus, D Seedburgh
• Pfeiffer syndrome: report of a family and review of the literature. (1 August, 1976)

  Y Naveh, A Friedman
• Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome: dominant inheritance and variable expression. (1 August, 1976)

  V B Penchaszadeh, T C de Negrotti
• Chronic spinal muscular atrophy of facioscapulohumeral type. (1 August, 1976)

  T Furukawa, Y Toyokura
• Genetic analyses of pyloric stenosis suggesting a specific maternal effect. (1 August, 1976)

  K K Kidd, M A Spence
• Chromosome survey of total population of mentally subnormal in North-East of Scotland. (1 August, 1976)

  R M Speed, A W Johnston, H J Evans
• Alkaline phosphatase activity in cultured skin fibroblasts from fibrodysplasia ossificans progressiva. (1 August, 1976)

  N G Beratis, S Kaffe, A M Aron, K Hirschhorn
• Topographic approach for analysis of palm crease variants. (1 August, 1976)

  H Dar, R Schmidt
• Further studies on the genetic heterogeneity of cebocephaly. (1 August, 1976)

  G I Lazjuk, I W Lurie, M K Nedzved
• X mapping in man: evidence against direct measurable linkage between ocular albinism and deutan colour blindness. (1 August, 1976)

  W G Pearce, R Sanger
• Non-disjunction of an unusual X chromosome. (1 August, 1976)

  I Hayata, M Oshimura, M J Marinello, R M Bannerman, A A Sandberg
• Reciprocal translocation, 4q-; 21p+, giving rise to Down's syndrome. (1 August, 1976)

  M B Jenkins, L Boyd
• Multiple congenital defects associated with trisomy for long arm of No. 4. (1 August, 1976)

  M Issa, A M Potter, C E Blank
• Tetraploidy in a liveborn infant. (1 August, 1976)

  M S Golbus, R Bachman, S Wiltse, B D Hall
• 46,XY/46,XY,21q- mosaicism in an infant with neutropenia and properdin deficiency. (1 August, 1976)

  R L Neu, J A Stockman, R E Spitzer, R H Tomar