Table of contents

Research Article

• Editorial postscript: 10 years of change and evolution. (1 May, 1995)

  P S Harper
• Familial pancreatic adenocarcinoma: association with diabetes and early molecular diagnosis. (1 May, 1995)

  J P Evans, W Burke, R Chen, R L Bennett, R A Schmidt, E P Dellinger, M Kimmey, D Crispin, T A Brentnall, D R Byrd
• Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village. (1 May, 1995)

  S Winata, I N Arhya, S Moeljopawiro, J T Hinnant, Y Liang, T B Friedman, J H Asher
• Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study. (1 May, 1995)

  U Drugge, M Holmberg, G Holmgren, B G Almay, H Linderholm
• Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness. (1 May, 1995)

  H Jensen, M Warburg, O Sjö, M Schwartz
• Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome. (1 May, 1995)

  N J Froggatt, J Koch, R Davies, D G Evans, A Clamp, O W Quarrell, J Weissenbach, S V Hodgson, B A Ponder, D E Barton
• Cognitive performance in UK sample of presymptomatic people carrying the gene for Huntington's disease. (1 May, 1995)

  L Blackmore, S A Simpson, J R Crawford
• Association between high serum total IgE levels and D11S97 on chromosome 11q13 in Japanese subjects. (1 May, 1995)

  N Hizawa, E Yamaguchi, K Furuya, N Ohnuma, N Kodama, J Kojima, M Ohe, Y Kawakami
• Craniometaphyseal dysplasia (CMD), autosomal dominant form. (1 May, 1995)

  P Beighton
• Bilateral split hand/foot malformation and inv(7)(p22q21.3). (1 May, 1995)

  J M Cobben, J B Verheij, W H Eisma, P H Robinson, R P Zwierstra, B Leegte, S Castedo
• Screening for mutations in exon 4 of the LDL receptor gene: identification of a new deletion mutation. (1 May, 1995)

  L Theart, M J Kotze, E Langenhoven, O Loubser, A V Peeters, C J Lintott, R S Scott
• X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome. (1 May, 1995)

  A K Gedeon, M J Wilson, A C Colley, D O Sillence, J C Mulley
• Linkage analysis of a large pedigree with hereditary sideroblastic anaemia. (1 May, 1995)

  J S Noble, G R Taylor, M S Losowsky, R Hall, G Turner, R F Mueller, A D Stewart
• Phenotypic variability in patients with generalised resistance to thyroid hormone. (1 May, 1995)

  J Pohlenz, S Wirth, A Winterpacht, H Wemme, B Zabel, W Schönberger
• Oguchi disease: suggestion of linkage to markers on chromosome 2q. (1 May, 1995)

  M A Maw, S John, S Jablonka, B Müller, G Kumaramanickavel, R Oehlmann, M J Denton, A Gal
• Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomes. (1 May, 1995)

  C Pêcheux, J F Mouret, A Dürr, Y Agid, J Feingold, A Brice, C Dodé, J C Kaplan
• A family study describing second cousins with cystic fibrosis and no common ancestor who is a carrier. (1 May, 1995)

  V M Park, M E Smith, M T Knight, M J Rock
• A comparison of the Huntington's disease associated trinucleotide repeat between Chinese and white populations. (1 May, 1995)

  B W Soong, J T Wang
• Rare variants of chromosome 9 with extra G positive band within the qh region are not alike. (1 May, 1995)

  R A Conte, S Gupta, J P Brennan, R S Verma
• Mild cystic fibrosis phenotype in patients with the 3272-26A > G mutation. (1 May, 1995)

  E Kanavakis, M Tzetis, T Antoniadi, J Trager-Synodinos, C Kattamis, S Doudounakis, G Adam