Table of contents

Research Article

• Gene mapping and medical genetics. (1 August, 1985)

  P S Harper
• Molecular genetics of the human X chromosome. (1 August, 1985)

  K E Davies
• A population study of adult onset limb-girdle muscular dystrophy. (1 August, 1985)

  J R Yates, A E Emery
• A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology. (1 August, 1985)

  S Bundey, T P Webb, A Thake, J Todd
• Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder. (1 August, 1985)

  R A Pagon, T D Bird, J C Detter, I Pierce
• The inheritance of primary lymphoedema. (1 August, 1985)

  R F Dale
• Zygosity determination in newborn twins using DNA variants. (1 August, 1985)

  C Derom, E Bakker, R Vlietinck, R Derom, H Van den Berghe, M Thiery, P Pearson
• A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome. (1 August, 1985)

  J L Watt, I A Olson, A W Johnston, H S Ross, D A Couzin, G S Stephen
• Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace. (1 August, 1985)

  M Aksoy, A Kutlar, F Kutlar, G Dinçol, S Erdem, S Baştesbihçi
• Admission of Hb S heterozygotes to a general hospital is relatively reduced in malarial areas. (1 August, 1985)

  B Colombo, L Felicetti
• Evaluation of haematological findings in 50 Bahraini patients with sickle cell disease and in some of their parents. (1 August, 1985)

  M A Buhazza, A B Bikhazi, F P Khouri
• Cornelia de Lange syndrome in several members of the same family. (1 August, 1985)

  D Kumar, C E Blank, B L Griffiths
• High incidence of Meckel's syndrome in Gujarati Indians. (1 August, 1985)

  I D Young, A B Rickett, M Clarke
• Gene deletion in an Italian haemophilia B subject. (1 August, 1985)

  F Bernardi, L del Senno, R Barbieri, D Buzzoni, R Gambari, G Marchetti, F Conconi, F Panicucci, M Positano, S Pitruzzello
• Two brothers with Martsolf's syndrome. (1 August, 1985)

  J M Sánchez, C Barreiro, H Freilij
• Familial pulmonary valve stenosis, atrial septal defect, and unique electrocardiogram abnormalities. (1 August, 1985)

  A A Ciuffo, E Cunningham, T A Traill
• Complex translocation in a boy with trichorhinophalangeal syndrome. (1 August, 1985)

  L M Sánchez, J D Labarta, T C De Negrotti, A M Migliorini
• Interstitial deletion of chromosome 7p detected antenatally. (1 August, 1985)

  K Marks, L Hill, R G Chitham, W L Whitehouse
• A possible mechanism underlying the sex selectivity of neural tube defect. (1 August, 1985)

  W H James
• Clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfecta. (1 August, 1985)

  J P Gage
• HLA antigens in South African Afrikaners with heterozygous familial hypercholesterolaemia. (1 August, 1985)

  S G Baker, A Rabson, R Shires, B I Joffe, H C Seftel
• Prenatal screening for Down syndrome. (1 August, 1985)

  M J Seller