Table of contents

Research Article

• A possible human homologue for the mouse mutant disorganisation. (1 July, 1989)

  R M Winter, D Donnai
• Disorganisation: a model for 'early amnion rupture'? (1 July, 1989)

  D Donnai, R M Winter
• Testing for cystic fibrosis using allelic association. (1 July, 1989)

  A J Ivinson, A P Read, R Harris, M Super, M Schwarz, J Clayton Smith, R Elles
• T cell receptor beta chain polymorphisms are associated with cystic fibrosis. (1 July, 1989)

  S A McMillan, A J Hill, C A Graham, N C Nevin, A C Fay
• Blepharophimosis plus ovarian failure: a likely candidate for a contiguous gene syndrome. (1 July, 1989)

  A Smith, I S Fraser, R P Shearman, P Russell
• Fragile X testing in a diagnostic cytogenetics laboratory. (1 July, 1989)

  L E Voullaire, G C Webb, M Leversha
• Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys. (1 July, 1989)

  L M Curfs, G Schreppers-Tijdink, A Wiegers, M Borghgraef, J P Fryns
• Severe Silver-Russell syndrome. (1 July, 1989)

  D Donnai, E Thompson, J Allanson, M Baraitser
• Differential expression of the ICF (immunodeficiency, centromeric heterochromatin, facial anomalies) mutation in lymphocytes and fibroblasts. (1 July, 1989)

  P Maraschio, R Tupler, E Dainotti, M Piantanida, G Cazzola, L Tiepolo
• Kyphomelic dysplasia. (1 July, 1989)

  I K Temple, E M Thompson, C M Hall, G Bridgeman, M E Pembrey
• A case of two inversion (10) recombinants in a family. (1 July, 1989)

  P Roberts, J Williams, M A Sills
• Sibs lacking characteristic features of duplication of distal 17q. (1 July, 1989)

  S Ohdo, H Madokoro, T Sonoda, K Ohba
• Ring chromosome 15 in a patient with features of Fryns' syndrome. (1 July, 1989)

  G de Jong, R A Rossouw, A E Retief
• Unknown syndrome: Noonan-like craniofacial features, digital anomalies, and premature birth. (1 July, 1989)

  R C Shepherd, D R Goudie, J L Tolmie
• The SHORT syndrome: further delineation and natural history. (1 July, 1989)

  A H Lipson, C Cowell, R J Gorlin