Table of contents

Research Article

• A genetic register for Huntington's chorea in South Wales. (1 August, 1982)

  P S Harper, A Tyler, S Smith, P Jones, R G Newcombe, V McBroom
• A three generation family study of cleft lip with or without cleft palate. (1 August, 1982)

  C O Carter, K Evans, R Coffey, J A Roberts, A Buck, M F Roberts
• Measurement of erythrocyte membrane elasticity as a diagnostic aid in Duchenne muscular dystrophy. (1 August, 1982)

  G B Nash, S J Wyard
• Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosa. (1 August, 1982)

  L L Field, J R Heckenlively, R S Sparkes, C A Garcia, C Farson, D Zedalis, M C Sparkes, M Crist, S Tideman, M A Spence
• Screening for latent acute intermittent porphyria: the value of measuring both leucocyte delta-aminolaevulinic acid synthase and erythrocyte uroporphyrinogen-1-synthase activities. (1 August, 1982)

  K E McColl, M R Moore, G G Thompson, A Goldberg
• The incidence of Down's syndrome in Nigeria. (1 August, 1982)

  A A Adeyokunnu
• A family study of craniosynostosis, with probable recognition of a distinct syndrome. (1 August, 1982)

  C O Carter, K Till, V Fraser, R Coffey
• An unusual form of familial acrocephalosyndactyly. (1 August, 1982)

  I D Young, P S Harper
• Familial Poland anomaly. (1 August, 1982)

  T J David
• Human chromosomal heteromorphisms in American blacks. VI. Higher incidence of longer Y owing to non-fluorescent (nf) segment. (1 August, 1982)

  R S Verma, M Evans-McCalla, H Dosik
• X long arm deletion with oligomenorrhoea. (1 August, 1982)

  K Mijin, E Stolević, S Adzić, Z Laća, S Marković
• Cd branding studies in a homologous Robertsonian 13;13 translocation. (1 August, 1982)

  D R Romain, L Columbano-Green, J Sullivan, R H Smythe, O Gebbie, R Parfitt, C Chapman
• Micromelia, polysyndactyly, multiple malformations, and fragile bones in a stillborn child. (1 August, 1982)

  B F Carpenter, A G Hunter
• Pericentric inversion of chromosome 11 in one of two similar retarded brothers. (1 August, 1982)

  S L Einfeld, A Smith
• Two successive partial trisomies for opposite halves of chromosome 22 in a mother with a balanced translocation. (1 August, 1982)

  R P Bendel, S Baldinger, C Millard, D C Arthur
• Adjacent 2 translocation involving 13q and 21q. (1 August, 1982)

  W W Woolf, C L Bradshaw, H E Hoyme, K L Jones, O W Jones
• Ectodermal dysplasia in females. (1 August, 1982)

  N Freire-Maia, M Pinheiro
• Delineation of trisomy 9. (1 August, 1982)

  G S Frohlich
• Wishes of patients with retinitis pigmentosa concerning genetic counselling. (1 August, 1982)

  S Bundey, S J Crews