Table of contents

Research Article

• Molecular and cytogenetic studies of the Prader-Willi syndrome. (1 October, 1991)

  R J Trent, F Volpato, A Smith, R Lindeman, M K Wong, G Warne, E Haan
• Genetic counselling in facioscapulohumeral muscular dystrophy. (1 October, 1991)

  P W Lunt, P S Harper
• A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q. (1 October, 1991)

  M Upadhyaya, P W Lunt, M Sarfarazi, W Broadhead, J Daniels, M Owen, P S Harper
• Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis. (1 October, 1991)

  A H Bröcker-Vriends, F R Rosendaal, J C van Houwelingen, E Bakker, G J van Ommen, J J van de Kamp, E Briët
• Linkage analysis in adenomatous polyposis coli: the use of four closely linked DNA probes in 20 UK families. (1 October, 1991)

  M B Cachon-Gonzalez, J D Delhanty, J Burn, K Tsioupra, M B Davis, J Attwood, P Chapman
• Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria. (1 October, 1991)

  L Kalaydjieva, B Dworniczak, C Aulehla-Scholz, M Devoto, G Romeo, M Sturhmann, V Kucinskas, V Yurgelyavicius, J Horst
• A male with type I orofaciodigital syndrome. (1 October, 1991)

  J Goodship, J Platt, R Smith, J Burn
• Miller syndrome (postaxial acrofacial dysostosis): further evidence for autosomal recessive inheritance and expansion of the phenotype. (1 October, 1991)

  A L Ogilvy-Stuart, A C Parsons
• A new form of autosomal dominant arthrogryposis. (1 October, 1991)

  M M Lai, M A Tettenborn, J G Hall, L J Smith, A C Berry
• Cerebrocostomandibular syndrome in four sibs, two pairs of twins. (1 October, 1991)

  V Drossou-Agakidou, A Andreou, V Soubassi-Griva, M Pandouraki
• Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct entity. (1 October, 1991)

  C G Bönnemann, P Meinecke, H Reich
• Disorganisation: a possible cause of apparent conjoint twinning. (1 October, 1991)

  M A Petzel, R P Erickson
• A cystic fibrosis patient homozygous for the nonsense mutation R553X. (1 October, 1991)

  J Bal, M Stuhrmann, M Schloesser, J Schmidtke, J Reiss
• An animal model for maternal phenylketonuria. (1 October, 1991)

  C Roux, F Rey, S Lyonnet, S Nizard, N Mulliez, A Munnich
• The non-deletion type of alpha thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritance. (1 October, 1991)

  A O Wilkie, M E Pembrey, R J Gibbons, D R Higgs, M E Porteous, J Burn, R M Winter
• Leiomyosarcoma in a patient with trisomy 8 mosaicism. (1 October, 1991)

  W M Molenaar, B De Jong, E Van den Berg
• Further evidence for the location of the BPES gene at 3q2. (1 October, 1991)

  C E de Die-Smulders, J J Engelen, J M Donk, J P Fryns