Table of contents

Research Article

• HLA-B27 and spondyloarthropathy: value for early diagnosis? (1 July, 1995)

  J T Gran, G Husby
• FISH analysis on spontaneously arising micronuclei in the ICF syndrome. (1 July, 1995)

  M Stacey, M S Bennett, M Hulten
• Utilities for high throughput use of the single strand conformational polymorphism method: screening of 791 patients with familial hypercholesterolaemia for mutations in exon 3 of the low density lipoprotein receptor gene. (1 July, 1995)

  R Whittall, V Gudnason, G P Weavind, L B Day, S E Humphries, I N Day
• Emotional and functional impact of DNA testing on patients with symptoms of Huntington's disease. (1 July, 1995)

  J Jankovic, J Beach, T Ashizawa
• Ascertainment of myotonic dystrophy through cataract by selective screening. (1 July, 1995)

  A Kidd, P Turnpenny, K Kelly, C Clark, W Church, C Hutchinson, J C Dean, N E Haites
• The epidemiology of Huntington's disease in Northern Ireland. (1 July, 1995)

  P J Morrison, W P Johnston, N C Nevin
• Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q. (1 July, 1995)

  G Van Camp, M N Van Thienen, I Handig, B Van Roy, V S Rao, A Milunsky, A P Read, C T Baldwin, L A Farrer, M Bonduelle
• The impact of newborn screening on cystic fibrosis testing in Victoria, Australia. (1 July, 1995)

  M E Balnaves, L Bonacquisto, I Francis, J Glazner, S Forrest
• Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiency. (1 July, 1995)

  P J Hallam, D S Millar, M Krawczak, V V Kakkar, D N Cooper
• Confirmation of genetic heterogeneity in familial psoriasis. (1 July, 1995)

  D Matthews, L Fry, A Powles, J Weissenbach, R Williamson
• Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS. (1 July, 1995)

  J C Ruiz, H Cuppens, E Legius, J P Fryns, T Glover, P Marynen, J J Cassiman
• Identification of constitutively activating mutation of the luteinising hormone receptor in a family with male limited gonadotrophin independent precocious puberty (testotoxicosis). (1 July, 1995)

  N Kawate, G B Kletter, B E Wilson, M L Netzloff, K M Menon
• Right upper limb bud triplication and polythelia, left sided hemihypertrophy and congenital hip dislocation, facial dysmorphism, congenital heart disease, and scoliosis: disorganisation-like spectrum or patterning gene defect? (1 July, 1995)

  M A Sabry, Q al-Saleh, R al-Saw'an, S A al-Awadi, T I Farag
• A fetus with an X;1 balanced reciprocal translocation and eye disease. (1 July, 1995)

  M J Seller, K Pal, S Horsley, A F Davies, A C Berry, R Meredith, A C McCartney
• Cerebellar atrophy in a patient with velocardiofacial syndrome. (1 July, 1995)

  D R Lynch, D M McDonald-McGinn, E H Zackai, B S Emanuel, D A Driscoll, L A Whitaker, K H Fischbeck
• Molecular analysis of three patients with interstitial deletions of chromosome band 14q31. (1 July, 1995)

  B C Byth, M T Costa, I E Teshima, W G Wilson, N P Carter, D W Cox
• Rapid detection of rare variants and common polymorphisms in the APC gene by PCR-SSCP for presymptomatic diagnosis and showing allele loss. (1 July, 1995)

  S A Gayther, R Sud, D Wells, K Tsioupra, J D Delhanty
• Chromosomal localisation of a Y specific growth gene(s). (1 July, 1995)

  T Ogata, K Tomita, A Hida, N Matsuo, Y Nakahori, Y Nakagome
• High incidence of delta I507 mutation of the CFTR gene in a limited area of the north west of France. (1 July, 1995)

  H Mittre, P Leymarie, N Leporrier
• Allele distribution of a highly polymorphic repeat on chromosome 12 in patients with symptoms of chorea and ataxia. (1 July, 1995)

  C Zühlke, O Knobloch, S Wagner, R Hilgers
• Detection of Y mosaicism in patients with Turner's syndrome. (1 July, 1995)

  C E Chu, J M Connor, M D Donaldson, C J Kelnar, P J Smail, S A Greene