Table of contents

Research Article

• The calcitonin-CGRP gene in the infantile hypercalcaemia/Williams-Beuren syndrome. (1 October, 1989)

  G A Hitman, L Garde, W Daoud, G J Snodgrass
• The molecular basis of beta thalassaemia in Bulgaria. (1 October, 1989)

  L Kalaydjieva, A Eigel, J Horst
• A summary of 7q interstitial deletions and exclusion mapping of the gene for beta-glucuronidase. (1 October, 1989)

  K Fagan, A Gill, R Henry, I Wilkinson, B Carey
• Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorder. (1 October, 1989)

  H Rivera, O Zuffardi, P Maraschio, A Caiulo, C Anichini, R Scarinci, R Vivarelli
• Transient nephrotic syndrome after anaesthesia resulting from a familial cryofibrinogen precipitating at 35 degrees C. (1 October, 1989)

  Y Lolin, P A Razis, P O'Gorman, M Hjelm, A S Wierzbicki
• Emery-Dreifuss syndrome. (1 October, 1989)

  A E Emery
• Familial mental retardation associated with balanced chromosome rearrangement rcp t(8;11)(q24.3;p15.1). (1 October, 1989)

  H Sato, K Takaya, S Nihira, H Fujita
• A new interstitial deletion of 4q (q21.1::q22.1). (1 October, 1989)

  K Fagan, A Gill
• Cat eye syndrome associated with aganglionosis of the small and large intestine. (1 October, 1989)

  J Ward, I A Sierra, E D'Croz
• A single maxillary incisor as a manifestation of an ectodermal dysplasia. (1 October, 1989)

  I Buntinx, M Baraitser
• Interstitial deletion, del(4)(q33q35.1), in a mother and two children. (1 October, 1989)

  M A Curtis, R A Smith, J Sibert, H E Hughes
• Maternal translocation (9;18) with two abnormal offspring each with different chromosome derivatives. (1 October, 1989)

  M Pearson, C Riske, J E Allanson
• Central nervous system malformations in Mohr's syndrome. (1 October, 1989)

  W Reardon, M G Harbord, M A Hall-Craggs, B Kendall, E M Brett, M Baraitser
• Unknown syndrome: congenital heart disease, ptosis, hypodontia, and craniosynostosis. (1 October, 1989)

  L Mehta, I Lewis, M A Patton
• Unknown syndrome in sibs: microcephaly, seizures, mental retardation, congenital heart disease, and skeletal abnormalities. (1 October, 1989)

  G E Holmes, R N Schimke
• Updated results of the thalassaemia prevention programme carried out in Latium. (1 October, 1989)

  I Bianco, B Graziani, M Lerone, D Ponzini, M C Aliquo, E Foglietta