Table of contents

Research Article

• Pancreatic function and gene deletion F508 in cystic fibrosis. (1 November, 1990)

  G Borgo, G Mastella, P Gasparini, A Zorzanello, R Doro, P F Pignatti
• Adrenoleucodystrophy: a molecular genetic study in five families. (1 November, 1990)

  R G Del Mastro, S Bundey, M W Kilpatrick
• In vitro gene amplification for prenatal diagnosis of congenital adrenal hyperplasia. (1 November, 1990)

  G Rumsby, J W Honour
• Deletion analysis of DMD/BMD families from the German Democratic Republic and selected regions of Czechoslovakia and Hungary. (1 November, 1990)

  A Speer, U Kräft, R Hanke, K Grade, C Coutelle, K Wulff, M Wehnert, F H Herrmann, L Kadasi, E Kunert
• Theoretical considerations on germline mosaicism in Duchenne muscular dystrophy. (1 November, 1990)

  T Grimm, B Müller, C R Müller, M Janka
• MASA syndrome: new clinical features and linkage analysis using DNA probes. (1 November, 1990)

  C Schrander-Stumpel, E Legius, J P Fryns, J J Cassiman
• Recessive metaphyseal dysplasia without hypotrichosis. A syndrome clinically distinct from McKusick cartilage-hair hypoplasia. (1 November, 1990)

  A Verloes, G E Pierard, M Le Merrer, P Maroteaux
• Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1. (1 November, 1990)

  S Kumar, W J Kimberling, P A Gabow, Y Y Shugart, S Pieke-Dahl
• Craniodiaphyseal dysplasia. (1 November, 1990)

  L A Brueton, R M Winter
• Teaching of clinical genetics in Britain: a report from the Royal College of Physicians of London. (1 November, 1990)

  A W Johnston
• Delivery of genetic services. (1 November, 1990)

  P S Harper
• Genetic services in Britain: a strategy for success after the National Health Service and Community Care Act 1990. (1 November, 1990)

  R Harris
• Familial congenital laryngeal abductor paralysis: different expression in a family with one male and three females affected. (1 November, 1990)

  A Schinzel, E Hof, P Dangel, W Robinson
• Ankyloblepharon filiforme adnatum in trisomy 18 Edwards syndrome. (1 November, 1990)

  D G Evans, I D Evans, D Donnai, R H Lindenbaum
• Triploidy arising from a first meiotic non-disjunction in a mother carrying a reciprocal translocation. (1 November, 1990)

  L Rochon, M J Vekemans
• Estimate of germinal mosaicism in Duchenne muscular dystrophy. (1 November, 1990)

  M R Passos-Bueno, M A Lima, M Zatz
• Identification of a balanced translocation carrier by spouse's low maternal serum alpha fetoprotein associated with an aneuploid fetus. (1 November, 1990)

  K Byrne-Essif, H E Hoyme