Table of contents

Research Article

• Alagille syndrome and deletion of 20p. (1 December, 1990)

  F Anad, J Burn, D Matthews, I Cross, B C Davison, R Mueller, M Sands, D M Lillington, E Eastham
• A 90 kb DNA deletion associated with neurofibromatosis type 1. (1 December, 1990)

  M Upadhyaya, A Cheryson, W Broadhead, A Fryer, D J Shaw, S Huson, M R Wallace, L B Andersen, D A Marchuk, D Viskochil
• Classical phenylketonuria in Bulgaria: RFLP haplotypes and frequency of the major mutations. (1 December, 1990)

  L Kalaydjieva, B Dworniczak, C Aulehla-Scholz, I Kremensky, J Bronzova, A Eigel, J Horst
• Two brothers with heart defects and limb shortening: case reports and review. (1 December, 1990)

  W Reardon, J Hurst, T I Farag, C Hall, M Baraitser
• Dilemmas in counselling: the EEC syndrome. (1 December, 1990)

  K Tse, I K Temple, M Baraitser
• Hydrolethalus syndrome. (1 December, 1990)

  R Salonen, R Herva
• Medical genetics in South Africa. (1 December, 1990)

  T Jenkins
• Anaphase lag as the most likely mechanism for monosomy X in direct cytotrophoblasts but not in mesenchymal core cells from the same villi. (1 December, 1990)

  M B Qumsiyeh, A T Tharapel, L P Shulman, J L Simpson, S Elias
• Tetraploidy in a liveborn infant. (1 December, 1990)

  I López Pajares, A Delicado, A Diaz de Bustamante, A Pellicer, I Pinel, M Pardo, M Martin
• Normal growth and development in a child with Baller-Gerold syndrome (craniosynostosis and radial aplasia). (1 December, 1990)

  P Galea, J L Tolmie
• Nasopharyngeal teratoma ('hairy polyp'), Dandy-Walker malformation, diaphragmatic hernia, and other anomalies in a female infant. (1 December, 1990)

  D J Aughton, C T Sloan, M P Milad, T E Huang, C Michael, C Harper
• Multiple pterygium syndrome: a relatively common disorder among Arabs. (1 December, 1990)

  A S Teebi, A S Daoud
• Features of Turner's and DiGeorge's syndromes with X;22 translocation. (1 December, 1990)

  S Gilgenkrantz, M Teboul
• Marfan syndrome. (1 December, 1990)

  R S Houlston, P Parry