Table of contents

Research Article

• Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome. (1 May, 1997)

  D Catchpoole, W W Lam, D Valler, I K Temple, J A Joyce, W Reik, P N Schofield, E R Maher
• The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q. (1 May, 1997)

  H Arnell, K Hjälmås, M Jägervall, G Läckgren, A Stenberg, B Bengtsson, C Wassén, T Emahazion, G Annerén, U Pettersson, M Sundvall, N Dahl
• Further delineation of Nevo syndrome. (1 May, 1997)

  L I al-Gazali, D Bakalinova, E Varady, J Scorer, M Nork
• Analysis of the 5' upstream sequence of the Huntington's disease (HD) gene shows six new rare alleles which are unrelated to the age at onset of HD. (1 May, 1997)

  R Coles, J Leggo, D C Rubinsztein
• Genotypic diagnosis of familial Mediterranean fever (FMF) using new microsatellite markers: example of two extensive non-Ashkenazi Jewish pedigrees. (1 May, 1997)

  M Dupont, C Dross, N Smaoui, B Nedelec, G Grateau, C Clépet, I Gourdier, I Koné-Paut, M Delpech, J Demaille, I Touitou
• Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics Workgroup. (1 May, 1997)

  A C DudokdeWit, A Tibben, H J Duivenvoorden, P G Frets, M W Zoeteweij, M Losekoot, A van Haeringen, M F Niermeijer, J Passchier
• Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease. (1 May, 1997)

  S Iyengar, H Kalinsky, S Weiss, M Korostishevsky, M Sadeh, Y Zhao, K K Kidd, B Bonne-Tamir
• Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome. (1 May, 1997)

  K Devriendt, P Petit, G Matthijs, J R Vermeesch, M Holvoet, A De Muelenaere, P Marynen, J J Cassiman, J P Fryns
• Ehlers-Danlos syndrome has varied molecular mechanisms. (1 May, 1997)

  F M Pope, N P Burrows
• Meiotic instability associated with the CAGR1 trinucleotide repeat at 13q13. (1 May, 1997)

  N T Potter
• Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects. (1 May, 1997)

  S B Dowton, A V Hing, V Sheen-Kaniecki, M S Watson
• Autosomal dominant inheritance of Weaver syndrome. (1 May, 1997)

  A Fryer, C Smith, L Rosenbloom, T Cole
• A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly. (1 May, 1997)

  D Steinberger, H Collmann, B Schmalenberger, U Müller
• Chromosome 22q11 deletion presenting as the Potter sequence. (1 May, 1997)

  K Devriendt, P Moerman, D Van Schoubroeck, K Vandenberghe, J P Fryns
• Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomy. (1 May, 1997)

  A Smith, R Marks, E Haan, J Dixon, R J Trent
• Interstitial deletion of band 3q25. (1 May, 1997)

  A M Slavotinek, S M Huson, M Fitchett
• Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patients. (1 May, 1997)

  H Arboleda, L Quintero, E Yunis