Table of contents

Research Article

• Blot hybridisation analysis of genomic DNA. (1 June, 1984)

  S Vandenplas, I Wiid, A Grobler-Rabie, K Brebner, M Ricketts, G Wållis, A Bester, C Boyd, C Måthew
• Homozygosity for autosomal dominant Marfan syndrome. (1 June, 1984)

  J Chemke, R Nisani, A Feigl, R Garty, M Cooper, Y Bårash, D Duksin
• Carrier detection in the testicular feminisation syndrome: deficient 5 alpha-dihydrotestosterone binding in cultured skin fibroblasts from the mothers of patients with complete androgen insensitivity. (1 June, 1984)

  M B Hodgins, E M Duke, D Ring
• Impaired HLA capping capacity of peripheral blood lymphocytes in Duchenne muscular dystrophy. (1 June, 1984)

  A Sensi, A Venturoli, S Traniello, M Lucci, C Vullo, C Conighi, P L Mattiuz, O R Båricordi
• Risk estimates for neonatal myotonic dystrophy. (1 June, 1984)

  A Glånz, F C Fråser
• Orofaciodigital syndrome with mesomelic limb shortening. (1 June, 1984)

  J Burn, C Dezateux, C M Hall, M Baraitser
• Spondyloepiphyseal dysplasia tarda with progressive arthropathy. (1 June, 1984)

  S A Al-Awadi, T I Fårag, K Naguib, M Y El-Khalifa, A Cuschieri, G Hosny, M Zahran, A G Al-Ansari
• Clinical and cytogenetic diversity in Fanconi's anaemia. (1 June, 1984)

  G Duckworth-Rysiecki, M Hultén, J Mann, A M Taylor
• Cytological subdivision of the S phase of human cells in asynchronous culture. (1 June, 1984)

  J R Savage, R Prasad
• An analysis of the parental age effect for inv dup (15). (1 June, 1984)

  J M Connor, D H Gilmore
• Report of the Clinical Genetics Society Working Party on the role and training of clinical geneticists, September 1983. (1 June, 1984)

  R Harris
• Fragile site at 12q13 associated with phenotypic abnormalities. (1 June, 1984)

  S Morić-Petrović, Z Laca
• A case of partial monosomy 21q22.2 associated with Rieger's syndrome. (1 June, 1984)

  F Nielsen, L Trånebjaerg
• Inv dup (15) with mental retardation but few dysmorphic features. (1 June, 1984)

  D H Gilmore, E Boyd, J P McClure, P Batstone, J M Connor
• Interstitial deletion of the short arm of chromosome 4. (1 June, 1984)

  M Ray, J Evans, C Rockman-Greenberg, D Wickstrom
• An unbalanced (6q;13q) translocation in a male with clinical features of Ehlers-Danlos type II syndrome. (1 June, 1984)

  P R Scarbrough, J Daw, A J Carroll, S C Finley
• Mosaic hexasomy 21. (1 June, 1984)

  A Ketupånyå, B F Crandåll, K Blanchard, D W Rogers
• De novo translocation involving chromosomes 2, 8, and 20. (1 June, 1984)

  D V Zaletajev, G S Marincheva, T G Tsvetkova
• 49,XXYY, +18 in a liveborn male. (1 June, 1984)

  G C Webb, E J Krumins, M A Leversha, G W Ford
• Ring (13),t(2;6) associated with familial fragile (16). (1 June, 1984)

  V Ventruto, A Rinaldi, S Renda, M Stabile, M M Rinaldi, M L Cavaliere, N Conte, V Aveta
• Whole arm translocation t(1;13) in an infertile man. (1 June, 1984)

  N Moreau, M Teyssier