Table of contents

Research Article

• Forensic medicine and the polymerase chain reaction technique. (1 August, 1993)

  R Decorte, J J Cassiman
• Association versus linkage studies in psychosis genetics. (1 August, 1993)

  M M Nöthen, P Propping, R Fimmers
• Association and linkage: complementary strategies for complex disorders. (1 August, 1993)

  M J Owen, P McGuffin
• Genetic transmission of Alzheimer's disease among families in a Dutch population based study. (1 August, 1993)

  C M van Duijn, L A Farrer, L A Cupples, A Hofman
• Origins of the fragile X syndrome mutation. (1 August, 1993)

  M C Hirst, S J Knight, Z Christodoulou, P K Grewal, J P Fryns, K E Davies
• Is skewed X inactivation responsible for symptoms in female carriers for adrenoleucodystrophy? (1 August, 1993)

  E Watkiss, T Webb, S Bundey
• A new de novo mutation (A113T) in HMG box of the SRY gene leads to XY gonadal dysgenesis. (1 August, 1993)

  Y T Zeng, Z R Ren, M L Zhang, Y Huang, F Y Zeng, S Z Huang
• Sequence variations in the first exon of alpha-galactosidase A. (1 August, 1993)

  J P Davies, B G Winchester, S Malcolm
• Classification of microphthalmos and coloboma. (1 August, 1993)

  M Warburg
• Impact of genetic counselling after neonatal screening for Duchenne muscular dystrophy. (1 August, 1993)

  E Hildes, H K Jacobs, A Cameron, S S Seshia, F Booth, J A Evans, K Wrogemann, C R Greenberg
• Evaluation of molecular genetic diagnosis in the management of familial adenomatous polyposis coli: a population based study. (1 August, 1993)

  E R Maher, D E Barton, R Slatter, D J Koch, M H Jones, H Nagase, S J Payne, S J Charles, A T Moore, Y Nakamura
• Cockayne's syndrome: correlation of clinical features with cellular sensitivity of RNA synthesis to UV irradiation. (1 August, 1993)

  A R Lehmann, A F Thompson, S A Harcourt, M Stefanini, P G Norris
• Campomelic dysplasia: evidence of autosomal dominant inheritance. (1 August, 1993)

  S A Lynch, M L Gaunt, A M Minford
• A three generation family with fibrodysplasia ossificans progressiva. (1 August, 1993)

  J M Connor, H Skirton, P W Lunt
• The substitution of glycine 661 by arginine in type III collagen produces mutant molecules with different thermal stabilities and causes Ehlers-Danlos syndrome type IV. (1 August, 1993)

  A Richards, P Narcisi, J Lloyd, C Ferguson, F M Pope
• A new form of familial ataxia, deafness, and mental retardation. (1 August, 1993)

  W Reardon, J Wilson, N Cavanagh, M Baraitser
• A new stable human dicentric chromosome, tdic(4;21)(p16;q22), in a woman with first trimester abortion. (1 August, 1993)

  F Wang, Y Li
• A new case of partial trisomy 19q (q13.2-->qter) owing to an unusual maternal translocation. (1 August, 1993)

  D Valerio, F Lavorgna, M Scalona, A Conte
• Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromes. (1 August, 1993)

  D Lacombe, F Serville, D Marchand, J Battin
• Dominant carpotarsal osteochondromatosis. (1 August, 1993)

  P Maroteaux, M Le Merrer, H Bensahel, P Freisinger
• Excess of homozygosity at the dopamine D3 receptor gene in schizophrenia not confirmed. (1 August, 1993)

  M M Nöthen, S Cichon, P Propping, R Fimmers, S G Schwab, D B Wildenauer
• Association between schizophrenia and homozygosity at the dopamine D3 receptor gene. (1 August, 1993)

  R T Morell
• Severity of chest disease in CF patients in relation to their genotypes. (1 August, 1993)

  G E Packe, Z H Miedzybrodzka, J C Dean