Table of contents

Research Article

• Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problems. (1 June, 1979)

  P E Polani, E Alberman, B J Alexander, P F Benson, A C Berry, S Blunt, M G Daker, A H Fensom, D M Garrett, V M McGuire, J A Roberts, M J Seller, J D Singer
• Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis. (1 June, 1979)

  A G Whitelaw, P A Rogers, D A Hopkinson, H Gordon, P M Emerson, J H Darley, C Reid, M A Crawfurd
• Inherited anaemias in the Greek community of Cape Town. (1 June, 1979)

  R P Bonafede, M C Botha, P Beighton
• Hepatitis--Bs antigen in an isolated Indian population of southern Venezuela: a family study. (1 June, 1979)

  A Soyano, Z Layrisse, M Layrisse, J V Neel
• Studies in mice on the mutagenicity of two contraceptive drugs. (1 June, 1979)

  M E Wallace, F M Badr, R S Badr
• May spina bifida result from an X-linked defect in a selective abortion mechanism? (1 June, 1979)

  J Burn, D Gibbens
• Two balanced translocations in three generations of a pedigree: t(7;10) (q11;q22) and t(14;21) (14qter to cen to 21qter)1. (1 June, 1979)

  H N Bass, R S Sparkes
• No increased chromosome breakage in three Bloom's syndrome heterozygotes. (1 June, 1979)

  E M Kuhn, E Therman
• X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency. (1 June, 1979)

  G Filippi, A Rinaldi, G Crisponi, G L Daniels, M Siniscalco
• Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis. (1 June, 1979)

  A Rinaldi, N Archidiacono, M Rocchi, G Filippi
• Normal phenotype and partial trisomy for the G positive region of chromosome 21. (1 June, 1979)

  A Daniel
• Trisomy 20p from maternal t(3;20) translocation. (1 June, 1979)

  N Archidiacono, D Tecilazich, G Tonini, M Rocchi, G Filippi
• Triple mosaicism 45,XY,--18/46, XY/47,XY,+18. (1 June, 1979)

  M Frydman, F Shabtai, Y Barak, I Halbrecht, E Elian
• The Prader-Willi syndrome with a 15/3 translocation. (1 June, 1979)

  M Kucerová, M Straková, Z Polívková
• Hereditary brachydactyly with nail dysplasia. (1 June, 1979)

  G D Schott
• The Rieger syndrome. (1 June, 1979)

  R J Jorgenson, F E Yoder, L S Levin