Table of contents

Research Article

• Prenatal diagnosis of osteogenesis imperfecta by identification of the concordant collagen 1 allele. (1 March, 1991)

  J R Lynch, D Ogilvie, L Priestley, C Baigrie, R Smith, P Farndon, B Sykes
• A cytogenetic and molecular study of a series of 45,X fetuses and their parents. (1 March, 1991)

  A Cockwell, M MacKenzie, S Youings, P Jacobs
• Analysis of the origin of Turner's syndrome using polymorphic DNA probes. (1 March, 1991)

  S A Loughlin, A Redha, J McIver, E Boyd, A Carothers, J M Connor
• Molecular studies of non-disjunction in trisomy 16. (1 March, 1991)

  T J Hassold, D Pettay, S B Freeman, M Grantham, N Takaesu
• Molecular and cytogenetic analysis of a familial microdeletion of Xq. (1 March, 1991)

  S Wells, S Mould, D Robins, D Robinson, P Jacobs
• Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene. (1 March, 1991)

  Y T Zeng, M J Chen, Z R Ren, X K Qui, S Z Huang
• Restriction fragment length polymorphisms associated with the factor VIII and factor IX genes in Polynesians. (1 March, 1991)

  N S Van-de-Water, D Ridgway, P A Ockelford
• Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish population. (1 March, 1991)

  E C Landels, I H Ellis, A H Fensom, P M Green, M Bobrow
• Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia. (1 March, 1991)

  P J Crawford, M J Aldred, A Clarke
• Dwarfism with gloomy face: a new syndrome with features of 3-M syndrome. (1 March, 1991)

  M Le Merrer, R Brauner, P Maroteaux
• The acetylator phenotypes of Saudi Arabians with coronary arterial atheroma. (1 March, 1991)

  D A Evans, J Wicks, J Higgins, M Assisto
• Analysis of problems in making the reproductive decision after genetic counselling. (1 March, 1991)

  P G Frets, H J Duivenvoorden, F Verhage, B M Peters-Romeyn, M F Niermeijer
• Floating-Harbor syndrome. (1 March, 1991)

  M A Patton, J Hurst, D Donnai, C M McKeown, T Cole, J Goodship
• A new case of proximal 10q partial trisomy. (1 March, 1991)

  M I de Michelena, P J Campos
• The CHARGE association and athyreosis. (1 March, 1991)

  J F Marín, B García, A Quintana, R Barrio, M T Sordo, C Lozano
• DMD carrier detection in a female with mosaic Turner's syndrome. (1 March, 1991)

  M Baiget, E Tizzano, V Volpini, E del Rio, T Pérez-Vidal, P Gallano
• Male proband with X linked retinoschisis apparently inherited from his father's family. (1 March, 1991)

  M S Newton, S Collyer, C I Phillips
• Child naevus is not ILVEN. (1 March, 1991)

  R Happle
• The variable clinical spectrum and mental prognosis of the acrocallosal syndrome. (1 March, 1991)

  J P Fryns, A Spaepen, C Grubben, H van den Berghe, P Casaer