Table of contents

Research Article

• Instability versus predictability: the molecular diagnosis of myotonic dystrophy. (1 November, 1992) Free

  G K Suthers, S M Huson, K E Davies
• Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations. (1 November, 1992) Free

  J Davies, H Yamagata, P Shelbourne, J Buxton, T Ogihara, P Nokelainen, M Nakagawa, R Williamson, K Johnson, T Miki
• Minimal expression of myotonic dystrophy: a clinical and molecular analysis. (1 November, 1992) Free

  W Reardon, H G Harley, J D Brook, S A Rundle, S Crow, P S Harper, D J Shaw
• The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy. (1 November, 1992) Free

  A Hunter, C Tsilfidis, G Mettler, P Jacob, M Mahadevan, L Surh, R Korneluk
• Presymptomatic diagnosis of myotonic dystrophy. (1 November, 1992) Free

  H G Brunner, W Nillesen, B A van Oost, G Jansen, B Wieringa, H H Ropers, H J Smeets
• Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. (1 November, 1992) Free

  J Myring, A L Meredith, H G Harley, G Kohn, G Norbury, P S Harper, D J Shaw
• Expansion of the myotonic dystrophy gene in Italian and Spanish patients. (1 November, 1992) Free

  S Melchionda, A Cobo, M Gennarelli, L Martorell, C Fattorini, M Baiget, A Lopez de Munain, K Johnson, P Shelbourne, G Novelli
• Intestinal pseudo-obstruction in myotonic dystrophy. (1 November, 1992) Free

  H G Brunner, B C Hamel, P Rieu, C J Höweler, F T Peters
• Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation. (1 November, 1992) Free

  D Heitz, D Devys, G Imbert, C Kretz, J L Mandel
• Frequent small amplifications in the FMR-1 gene in fra(X) families: limits to the diagnosis of 'premutations'. (1 November, 1992) Free

  J N Macpherson, D L Nelson, P A Jacobs
• Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group. (1 November, 1992) Free

  A Brice, N Ravisé, G Stevanin, M Gugenheim, P Bouche, C Penet, Y Agid
• High frequency of the Lebanese allele of the LDLr gene among Brazilian patients with familial hypercholesterolaemia. (1 November, 1992) Free

  M S Figueiredo, J E Dos Santos, F L Alberto, M A Zago
• Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease). (1 November, 1992) Free

  G Wolff, A Mayerová, T F Wienker, P Atalianis, P Ioannou, M Warburg
• Factors affecting the uptake of prenatal diagnosis for sickle cell disease. (1 November, 1992) Free

  M Petrou, M Brugiatelli, R H Ward, B Modell
• Polyglandular autoimmune syndrome type I among Iranian Jews. (1 November, 1992) Free

  J Zlotogora, M S Shapiro
• Orofaciodigital syndrome type I in a girl with unilateral tibial pseudarthrosis. (1 November, 1992) Free

  K H Orstavik, S E Tangsrud, T Nordshus, A M Finnanger, C Hellum, E Gjessing
• Lethal skeletal dysplasia owing to double heterozygosity for achondroplasia and spondyloepiphyseal dysplasia congenita. (1 November, 1992) Free

  I D Young, N R Ruggins, J M Somers, J M Zuccollo, N Rutter
• An atypical form of mucolipidosis III. (1 November, 1992) Free

  P Freisinger, J C Padovani, P Maroteaux