Table of contents

Research Article

• The genetic control of sparteine and debrisoquine metabolism in man with new methods of analysing bimodal distributions. (1 October, 1983)

  D A Evans, D Harmer, D Y Downham, E J Whibley, J R Idle, J Ritchie, R L Smith
• The association of the slow acetylator phenotype with bladder cancer. (1 October, 1983)

  D A Evans, L C Eze, E J Whibley
• Linkage analysis of neurofibromatosis (von Recklinghausen disease). (1 October, 1983)

  M A Spence, J L Bader, D M Parry, L L Field, S J Funderburk, A E Rubenstein, P A Gilman, R S Sparkes
• Congenital malformations associated with anencephaly in the Fylde peninsula of Lancashire. (1 October, 1983)

  T J David, F C McCrae, J P Bound
• Familial atypical multiple mole-melanoma (FAMMM) syndrome: segregation analysis. (1 October, 1983)

  H T Lynch, R M Fusaro, W J Kimberling, J F Lynch, B S Danes
• The infrequency of malignant disease in diaphyseal aclasis and neurofibromatosis. (1 October, 1983)

  S Voutsinas, R Wynne-Davies
• C heterochromatin variation in couples with recurrent early abortions. (1 October, 1983)

  A Maes, C Staessen, L Hens, E Vamos, M Kirsch-Volders, M C Lauwers, E Defrise-Gussenhoven, C Susanne
• Familial aggregation of streptomycin ototoxicity: autosomal dominant inheritance? (1 October, 1983)

  D L Viljoen, S L Sellars, P Beighton
• Constitutional aplastic anaemia: a family with a new X linked variety of amegakaryocytic thrombocytopenia. (1 October, 1983)

  A D Griffiths
• HLA-DR2 in two sibships with insulin-dependent diabetes mellitus. (1 October, 1983)

  I Deschamps, H Lestradet, M Schmid, J Hors
• Empirical recurrence risk after unidentified multiple congenital abnormalities. (1 October, 1983)

  A Czeizel, J Métneki
• Spontaneous and mutagen induced sister chromatid exchange in multiple sclerosis. (1 October, 1983)

  Vijayalaxmi, M S Newton, C M Steel, H J Evans, B Pentland
• Monosomy 18p and pure trisomy 18p in a family with translocation (7;18). (1 October, 1983)

  M Habedank, G Trost-Brinkhues
• Two cases of ring chromosome 11. (1 October, 1983)

  D R Romain, O B Gebbie, R G Parfitt, L M Columbano-Green, R H Smythe, C J Chapman, A Kerr
• A child with partial trisomy of chromosome 17 and partial monosomy of chromosome 3: 46,XY,der(3),t(3;17)(p25;q23). (1 October, 1983)

  D J Shawe, C Fear, W J Appleyard
• De novo translocation heterozygote with three reciprocal translocations. (1 October, 1983)

  J L Watt, D A Couzin
• A complex double translocation involving four chromosomes and five breakpoints in a child with mild mental retardation. (1 October, 1983)

  D A Couzin, J L Watt, I A Auchterlonie
• Yq deletion with short stature, abnormal male development, and schizoid character disorder. (1 October, 1983)

  G Kosztolányi, M Trixler
• Complete trisomy 5p owing to de novo translocation t(5;22)(q11;p11) with isochromosome 5p associated with a familial pericentric inversion of chromosome 2, inv 2(p21q11). (1 October, 1983)

  E Orye, Y Benoit, B van Mele
• Tetrasomy 9p confirmed by GALT. (1 October, 1983)

  P Balestrazzi, G Croci, C Frassi, F Franchi, G Giovannelli