Table of contents

Research Article

• Different options for prenatal testing for Huntington's disease using DNA probes. (1 June, 1989)

  M Fahy, C Robbins, M Bloch, R W Turnell, M R Hayden
• Clinical variability of osteogenesis imperfecta linked to COL1A2 and associated with a structural defect in the type I collagen molecule. (1 June, 1989)

  A Superti-Furga, F Pistone, C Romano, B Steinmann
• Prenatal diagnosis of beta thalassaemia based on restriction endonuclease analysis of amplified fetal DNA. (1 June, 1989)

  M Pirastu, M S Ristaldi, A Cao
• Ultrasound in the perinatal necropsy. (1 June, 1989)

  M E Furness, R C Weckert, S A Parker, S Knowles
• X linked mental retardation: a family with a separate syndrome? (1 June, 1989)

  E M Thompson, A Gordon, M Baraitser
• Chromosome studies of males in an institution for the mentally handicapped. (1 June, 1989)

  C J English, E V Davison, M S Bhate, L Barrett
• Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable association. (1 June, 1989)

  K D MacDermot, M A Patton, M J Williams, R M Winter
• Dominantly inherited cleft lip and palate in two families. (1 June, 1989)

  K Temple, M Calvert, D Plint, E Thompson, M Pembrey
• Population frequencies of three DNA alleles linked to the Duchenne muscular dystrophy gene. (1 June, 1989)

  S S Papiha, D F Roberts, A Clarke, J Burn, D Gardner-Medwin, S S Bhattacharya
• Cranioectodermal dysplasia (Sensenbrenner's syndrome). (1 June, 1989)

  I D Young
• Microcephaly, mental retardation, cataracts, and hypogonadism in sibs: Martsolf's syndrome. (1 June, 1989)

  M G Harbord, M Baraitser, J Wilson
• Dominant inheritance of Scheuermann's juvenile kyphosis. (1 June, 1989)

  A Findlay, A N Conner, J M Connor
• Prenatal diagnosis of the megacystis-microcolon-intestinal hypoperistalsis syndrome. (1 June, 1989)

  I D Young, P A McKeever, L A Brown, G D Lang
• Unknown syndrome: congenital heart disease, choanal stenosis, short stature, developmental delay, and dysmorphic facial features in a brother and sister. (1 June, 1989)

  J A Hurst, A C Berry, M A Tettenborn
• Frontonasal dysplasia, congenital heart defect, and short stature: a further observation. (1 June, 1989)

  P Meinecke, W Blunck
• Single base pair alterations as the predominant category of mutation in type I osteogenesis imperfecta. (1 June, 1989)

  A J Brookes, B Sykes, E Solomon
• Lethal osteogenesis imperfecta. (1 June, 1989)

  A S Knisely, D Abuelo, P H Byers
• Genetic heterogeneity in Waardenburg's syndrome. (1 June, 1989)

  M L Kulkarni, M Kurian, G Guruprasad, M S Panchakshariah
• Current trends in the prevalence at birth of neural tube defects in Singapore. (1 June, 1989)

  K C Tan, N K Ho