Table of contents

Research Article

• Linkage disequilibrium in Huntington's disease: an improved localisation for the gene. (1 November, 1989)

  R G Snell, L P Lazarou, S Youngman, O W Quarrell, J J Wasmuth, D J Shaw, P S Harper
• Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene. (1 November, 1989)

  J Theilmann, S Kanani, R Shiang, C Robbins, O Quarrell, M Huggins, A Hedrick, B Weber, C Collins, J J Wasmuth
• Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy. (1 November, 1989)

  S Hodgson, K Hart, S Abbs, J Heckmatt, E Rodillo, M Bobrow, V Dubowitz
• Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosis. (1 November, 1989)

  L I al-Gazali, R J Arthur, J T Lamb, H M Hammer, T P Coker, P N Hirschmann, J Gibbs, R F Mueller
• A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity. (1 November, 1989)

  S M Huson, D A Compston, P Clark, P S Harper
• A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling. (1 November, 1989)

  S M Huson, D A Compston, P S Harper
• Fountain's syndrome: mental retardation, sensorineural deafness, skeletal abnormalities, and coarse face with full lips. (1 November, 1989)

  J P Fryns
• Abnormal chromosome complement resulting from a familial inversion of chromosome 2. (1 November, 1989)

  S Richter, B Lockwood, D Lockwood, J Allanson
• Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic features. (1 November, 1989)

  L A Brueton, J C Barber, S M Huson, R M Winter
• Pituitary function studies in a case of mild Hunter's syndrome (MPS IIB). (1 November, 1989)

  J Nelson, D Carson
• Thanatophoric dysplasia in identical twins. (1 November, 1989)

  A S Knisely