Table of contents

Research Article

• Molecular genetics of human chromosome 4. (1 June, 1986)

  J A Gusella, T C Gilliam, M E MacDonald, S V Cheng, R E Tanzi
• Walker-Warburg syndrome (Warburg syndrome, HARD +/- E syndrome). (1 June, 1986)

  D Donnai, P A Farndon
• Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia. (1 June, 1986)

  G Rumsby, M C Carroll, R R Porter, D B Grant, M Hjelm
• DNA polymorphic haplotypes on the short arm of chromosome 11 and the inheritance of type I diabetes mellitus. (1 June, 1986)

  G A Ferns, G A Hitman, R Trembath, L Williams, A Tarn, E A Gale, D J Galton
• Exclusion of close linkage between the parathyroid hormone gene and a mutant gene locus causing idiopathic hypoparathyroidism. (1 June, 1986)

  J Schmidtke, K Kruse, B Pape, G Sippell
• The estimation of risks from the induction of recessive mutations after exposure to ionising radiation. (1 June, 1986)

  A G Searle, J H Edwards
• Risk of dominant mutation in older fathers: evidence from osteogenesis imperfecta. (1 June, 1986)

  A D Carothers, S J McAllion, C R Paterson
• Freeman-Sheldon syndrome: a disorder of congenital myopathic origin? (1 June, 1986)

  J Vanĕk, J Janda, V Amblerová, F Losan
• Type II syndactyly or synpolydactyly. (1 June, 1986)

  P Merlob, M Grunebaum
• Mental retardation associated with congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth. (1 June, 1986)

  S Ohdo, H Madokoro, T Sonoda, K Hayakawa
• Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia. (1 June, 1986)

  J M White, M Byrne, R Richards, T Buchanan, E Katsoulis, K Weerasingh
• Bone marrow and peripheral blood globin chain synthesis in sickle cell beta zero thalassaemia. (1 June, 1986)

  F F Costa, M A Zago
• Trisomy 18 in a 13 year old girl. (1 June, 1986)

  L Mehta, R S Shannon, D P Duckett, I D Young
• Prenatal detection of monosomy 18p and trisomy 18q mosaicism with unexpected fetal phenotype. (1 June, 1986)

  S D Sutton, M A Ridler
• Partial monosomy 13q and partial trisomy 18p: case report with necropsy findings. (1 June, 1986)

  D Beneck, M A Greco, S R Wolman, L E McMorrow, V Jansen, J Cason
• 18q+, the progeny of a balanced translocation t(1;18)mat: case report with necropsy findings. (1 June, 1986)

  A Hindi, D Beneck, M A Greco, S R Wolman
• Is reserpine a human teratogen? (1 June, 1986)

  R M Pauli, B J Pettersen
• Tel Hashomer camptodactyly syndrome: report of a case with myopathic features. (1 June, 1986)

  M A Patton, K D McDermot, B D Lake, M Baraitser
• A male infant with the Catel-Manzke syndrome and dislocatable knees. (1 June, 1986)

  E M Thompson, R M Winter, M J Williams
• Outcome after prenatal detection of a sporadic, unstable translocation t(5;21). (1 June, 1986)

  A O Martin, I Benuck, H S Traisman, M S Swanson, N Trakas, K Laing, B J Rosinsky, J Beaird, E S Traisman, S Elias
• A fragile site 10q25 in human sperm chromosomes. (1 June, 1986)

  R H Martin
• Did the Hb G San José gene arise in Sicily? (1 June, 1986)

  G Schilirò, S Li Volti