Table of contents

Research Article

• Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations. (1 February, 1995)

  P Riordan-Eva, A E Harding
• DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome. (1 February, 1995)

  G Gillessen-Kaesbach, S Gross, S Kaya-Westerloh, E Passarge, B Horsthemke
• Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele. (1 February, 1995)

  R J Daniels, L Campbell, N R Rodrigues, M J Francis, K E Morrison, M McLean, A MacKenzie, J Ignatius, V Dubowitz, K E Davies
• The prenatal exclusion test for Huntington's disease: experience in the west of Scotland, 1986-1993. (1 February, 1995)

  J L Tolmie, H R Davidson, H M May, K McIntosh, J S Paterson, B Smith
• Recurrence risk for germinal mosaics revisited. (1 February, 1995)

  M A van der Meulen, M J van der Meulen, G J te Meerman
• Contribution of molecular analyses to the estimation of the risk of congenital myotonic dystrophy. (1 February, 1995)

  A M Cobo, J J Poza, L Martorell, A López de Munain, J I Emparanza, M Baiget
• Cholinesterase variants: rapid characterisation by PCR/SSCP and evidence for molecular homogeneity. (1 February, 1995)

  T Höhler, M Hundt, C Rittner, P M Schneider, K H Meyer zum Büschenfelde
• Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation. (1 February, 1995)

  D F Callen, H J Eyre, G Dolman, M B Garry-Battersby, J R McCreanor, A Valeba, J J McGill
• Cowden syndrome. (1 February, 1995)

  A M Hanssen, J P Fryns
• DNA analysis of Huntington's disease in southern Chinese. (1 February, 1995)

  V Chan, Y L Yu, T P Chan, B Yip, C M Chang, M T Wong, Y W Chan, T K Chan
• Pallister-Hall syndrome and McKusick-Kaufmann syndrome: one entity? (1 February, 1995)

  K M Unsinn, N Neu, A Krejci, A Posch, G Menardi, I Gassner
• Modification of standard proteinase K/phenol method for DNA isolation to improve yield and purity from frozen blood. (1 February, 1995)

  N N Ahmad, A B Cu-Unjieng, L A Donoso
• A weak association between TH and DRD2 genes and bipolar affective disorder in a Spanish sample. (1 February, 1995)

  I Pérez de Castro, J Santos, P Torres, G Visedo, J Saiz-Ruiz, C Llinares, J Fernández-Piqueras
• British Medical Genetics Conference. York, 12-14 September 1994. Abstracts. (1 February, 1995)
• Two CF patients, one homozygous for the 621 + 1G > T splice mutation, the other homozygous for the 1898 + 1G > A splice mutation. (1 February, 1995)

  J P Cheadle, A L Meredith, L Millar-Jones, M C Goodchild