Table of contents

Research Article

• Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes. (1 January, 1989)

  A Speer, A W Spiegler, R Hanke, K Grade, U Giertler, J Schieck, S Forrest, K E Davies, R Neumann, R Bollmann
• Alpha thalassaemia: a potential source of error in DNA linkage studies for adult polycystic kidney disease. (1 January, 1989)

  R J Trent, R C Wallace
• 21-hydroxylase deficiency families with HLA identical affected and unaffected sibs. (1 January, 1989)

  P J Sinnott, P A Dyer, D A Price, R Harris, T Strachan
• New mutation to Huntington's disease. (1 January, 1989)

  G Wolff, G Deuschl, T F Wienker, K Hummel, K Bender, C H Lücking, M Schumacher, J Hammer, G Oepen
• Genetic aspects of tuberous sclerosis in the west of Scotland. (1 January, 1989)

  J R Sampson, S J Scahill, J B Stephenson, L Mann, J M Connor
• The use of low density lipoprotein receptor activity of lymphocytes to determine the prevalence of familial hypercholesterolaemia in a rural South African community. (1 January, 1989)

  K Steyn, M J Weight, B R Dando, K J Christopher, J E Rossouw
• Congenital generalised bone dysplasias: a clinical, radiological, and epidemiological survey. (1 January, 1989)

  P E Andersen, M Hauge
• Johanson-Blizzard syndrome. (1 January, 1989)

  J A Hurst, M Baraitser
• Congenital hypothyroidism, spiky hair, and cleft palate. (1 January, 1989)

  J S Bamforth, I A Hughes, J H Lazarus, C M Weaver, P S Harper
• Hydrocephalus, tall stature, joint laxity, and kyphoscoliosis: a new inherited disorder of connective tissue? (1 January, 1989)

  P Daish, M J Hardman, M A Lamont
• Further delineation of the Yunis-Varon syndrome. (1 January, 1989)

  R C Hennekam, C Vermeulen-Meiners
• A case of interstitial deletion of 10q25.2----q26.1. (1 January, 1989)

  D E Rooney, K Williams, D V Coleman, A Habel
• Deletion of chromosome 5q and familial adenomatous polyposis. (1 January, 1989)

  K A Hockey, M T Mulcahy, P Montgomery, S Levitt
• Obesity and abnormal behaviour associated with interstitial deletion of chromosome 18 (q12.2q21.1). (1 January, 1989)

  G N Wilson, A A Al Saadi
• Partial trisomy 16q secondary to a maternal 9;16 translocation. (1 January, 1989)

  M L Lessick, J Israel, P W Wong, K Szego
• Duplication 6p and deletion 9p. (1 January, 1989)

  C Lytle, J Wade, A Farrier, F Flohrschutz, B Hecht, J Allanson
• The megacystis-microcolon-intestinal hypoperistalsis syndrome: a fatal autosomal recessive condition. (1 January, 1989)

  D G Penman, R J Lilford
• Apple peel syndrome in sibs. (1 January, 1989)

  T I Farag, A S Teebi
• Iris coloboma, ptosis, hypertelorism, and mental retardation. (1 January, 1989)

  B D Hall
• Teratogenicity of ergotamine. (1 January, 1989)

  A Czeizel
• 18p- syndrome with partial sacral agenesis. (1 January, 1989)

  S Anderson-Shotwell, W G Wilson