Table of contents

Research Article

• Redrafted Chinese law remains eugenic. (1 June, 1995)

  M Bobrow
• Nuclear and mitochondrial genetics in Parkinson's disease. (1 June, 1995)

  A H Schapira
• A clinical and genetic study of campomelic dysplasia. (1 June, 1995)

  S Mansour, C M Hall, M E Pembrey, I D Young
• A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data. (1 June, 1995)

  B S Sayli, A N Akarsu, U Sayli, O Akhan, S Ceylaner, M Sarfarazi
• A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype? (1 June, 1995)

  A N Akarsu, O Akhan, B S Sayli, U Sayli, G Baskaya, M Sarfarazi
• DNA microsatellite analysis of families with autosomal dominant polycystic kidney disease types 1 and 2: evaluation of clinical heterogeneity between both forms of the disease. (1 June, 1995)

  E Coto, S Sanz de Castro, S Aguado, J Alvarez, M Arias, M J Menéndez, C López-Larrea
• Allelic associations and homozygosity at loci from HLA-B to D6S299 in genetic haemochromatosis. (1 June, 1995)

  R Raha-Chowdhury, D J Bowen, A K Burnett, M Worwood
• Epidemiology and genetics of microtia-anotia: a registry based study on over one million births. (1 June, 1995)

  P Mastroiacovo, C Corchia, L D Botto, R Lanni, G Zampino, D Fusco
• The dental phenotype in familial adenomatous polyposis: diagnostic application of a weighted scoring system for changes on dental panoramic radiographs. (1 June, 1995)

  N Thakker, R Davies, K Horner, J Armstrong, T Clancy, S Guy, R Harris, P Sloan, G Evans
• Neuroectodermal (CHIME) syndrome: an additional case with long term follow up of all reported cases. (1 June, 1995)

  V Shashi, J Zunich, T E Kelly, J S Fryburg
• Diagnostic issues in a family with late onset type 2 neurofibromatosis. (1 June, 1995)

  D G Evans, D Bourn, A Wallace, R T Ramsden, J D Mitchell, T Strachan
• Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastoma. (1 June, 1995)

  I Szijan, D R Lohmann, D L Parma, B Brandt, B Horsthemke
• H714Q mutation in Wilson disease is associated with late, neurological presentation. (1 June, 1995)

  R H Houwen, J Juyn, T U Hoogenraad, J K Ploos van Amstel, R Berger
• Inheritance of CMT1A duplication from a mosaic father. (1 June, 1995)

  E Sorour, P Thompson, J MacMillan, M Upadhyaya
• Good growth response to growth hormone treatment in the ring chromosome 15 syndrome. (1 June, 1995)

  M Nuutinen, K Kouvalainen, M Knip
• A new PAX6 mutation in familial aniridia. (1 June, 1995)

  I Hanson, A Brown, V van Heyningen
• GIG response to the UK Clinical Genetics Society report "The genetic testing of children". (1 June, 1995)

  S Dalby
• The genetic testing of children. (1 June, 1995)

  A Clarke
• Possible genetic heterogeneity in hypochondroplasia. (1 June, 1995)

  I Stoilov, M W Kilpatrick, P Tsipouras, T Costa
• UPD 13: no indication of maternal or paternal imprinting of genes on chromosome 13. (1 June, 1995)

  H Slater, J H Shaw, A Bankier, S M Forrest, G Dawson
• A family with autosomal dominant polycystic kidney disease linked to 4q21-23. (1 June, 1995)

  S Jeffery, S Morgan, V J Warmington, G A MacGregor, A K Saggar-Malik