Table of contents

Research Article

• The polymerase chain reaction: current and future clinical applications. (1 January, 1990)

  J R Lynch, J M Brown
• A consortium approach to molecular genetic services. Scottish Molecular Genetics Consortium. (1 January, 1990)

  D J Brock
• Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus. (1 January, 1990)

  C F Inglehearn, S S Papiha, M Jay, A F Wright, A T Moore, S S Bhattacharya
• The genotype of a new linked DNA marker, MP6d-9, is related to the clinical course of cystic fibrosis. (1 January, 1990)

  P Gasparini, G Novelli, X Estivill, D Olivieri, A Savoia, A Ruzzo, V Nunes, G Borgo, M Antonelli, R Williamson
• Search for consanguinity within and among families of patients with trichothiodystrophy associated with xeroderma pigmentosum. (1 January, 1990)

  F Nuzzo, G Zei, M Stefanini, R Colognola, A S Santachiara, P Lagomarsini, S Marinoni, L Salvaneschi
• A family study of congenital X linked sideroblastic anaemia. (1 January, 1990)

  J Holmes, A May, D Geddes, A Jacobs
• An epidemiological and genetic study of congenital profound deafness in Tunisia (governorate of Nabeul). (1 January, 1990)

  S Ben Arab, C Bonaïti-Pellié, A Belkahia
• Ethical issues policy statement on Huntington's disease molecular genetics predictive test. International Huntington Association. World Federation of Neurology. (1 January, 1990)

  L Went
• DNA markers near the cystic fibrosis locus: further analysis of the British population. (1 January, 1990)

  A Harris
• The Schinzel-Giedion syndrome. (1 January, 1990)

  L I al-Gazali, P Farndon, J Burn, D B Flannery, C Davison, R F Mueller
• The acrocallosal syndrome in a Turkish boy. (1 January, 1990)

  M Yüksel, M Caliskan, G Oğur, M Ozmen, G Dolunay, S Apak
• Holoprosencephaly and polydactyly: a possible expression of the hydrolethalus syndrome. (1 January, 1990)

  H Bachman, R D Clark, W Salahi
• Poland's syndrome associated with growth hormone deficiency. (1 January, 1990)

  D Larizza, M Maghnie
• De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies. (1 January, 1990)

  I K Temple, J A Hurst, S Hing, L Butler, M Baraitser
• Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3. (1 January, 1990)

  L I al-Gazali, R F Mueller, A Caine, A Antoniou, A McCartney, M Fitchett, N R Dennis
• Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a child with multiple congenital abnormalities. (1 January, 1990)

  M A Curtis, O W Quarrell, A M Cobon, M Cummins
• Application of a new DNA sequence polymorphism as a genetic marker in prenatal diagnosis of phenylketonuria. (1 January, 1990)

  S Z Huang, Z R Ren, Y T Zeng
• Polymerase chain reaction (PCR) on fixed necropsy material. (1 January, 1990)

  R F Mueller, G R Taylor, A D Stewart, J S Noble, P Quirke, G Batcup, A Ivinson
• Huntington's disease testing: what and what not to tell. (1 January, 1990)

  R J Gardner, G R Gillett, C J Chapman
• Options for prenatal testing for Huntington's disease using linked DNA probes. (1 January, 1990)

  D J Brock, A Curtis, M Mennie, J A Raeburn
• Oculocerebrocutaneous syndrome. (1 January, 1990)

  L M Bleeker-Wagemakers, B C Hamel, R C Hennekam, F A Beemer, H W Oorthuys