Table of contents

Research Article

• The molecular genetics of human chromosome 6. (1 November, 1987)

  V Cunliffe, J Trowsdale
• Hypohidrotic ectodermal dysplasia. (1 November, 1987)

  A Clarke
• Malignant melanoma in families of children with osteosarcoma, chondrosarcoma, and adrenal cortical carcinoma. (1 November, 1987)

  A L Hartley, J M Birch, H B Marsden, M Harris
• Variant forms of ataxia telangiectasia. (1 November, 1987)

  A M Taylor, E Flude, B Laher, M Stacey, E McKay, J Watt, S H Green, A E Harding
• The inheritance of fragile sites: apparent absence of fra(2)(q13) in the parents of three unrelated probands. (1 November, 1987)

  L Keskiaho, S Knuutila, H Pihko, A Nuutila, U Kaski, M Koivikko, A de la Chapelle
• Familial t(8;15)(p23.3;q22.3): report of two cases with dup(15) (q22.3----qter). (1 November, 1987)

  D J Goldstein, R E Ward, W C Nichols, C G Palmer
• Congenital anal anomalies in two families with the Opitz G syndrome. (1 November, 1987)

  J L Tolmie, N Coutts, I K Drainer
• Fetal valproate syndrome: is there a recognisable phenotype? (1 November, 1987)

  R M Winter, D Donnai, J Burn, S M Tucker
• Deletion (13)(q13q14.3) with retinoblastoma: confirmation and extension of a recognisable pattern of clinical features in retinoblastoma patients with 13q deletion. (1 November, 1987)

  T Motegi, K Ikeda, K Watanabe, Y Yanagawa, K Minoda
• The clinical features of Ehlers-Danlos syndrome type VII due to a deletion of 24 amino acids from the pro alpha 1(I) chain of type I procollagen. (1 November, 1987)

  W G Cole, R Evans, D O Sillence
• Spastic paraplegia associated with brachydactyly and cone shaped epiphyses. (1 November, 1987)

  J S Fitzsimmons, P R Guilbert
• Partial deletion 21: case report with biochemical studies and review. (1 November, 1987)

  N J Carpenter, J S Mayes, B Say, D P Wilson
• Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5. (1 November, 1987)

  M Y Yip, M Selikowitz, N Don, A Kovacic, S Purvis-Smith, P R Lam-Po-Tang
• Unknown syndrome: holoprosencephaly, congenital heart defects, and polydactyly. (1 November, 1987)

  I D Young, D J Madders
• Unknown syndrome: abnormal facies, congenital heart defects, hypothyroidism, and severe retardation. (1 November, 1987)

  I D Young, K Simpson