Table of contents

Research Article

• On the parental origin of de novo mutation in man. (1 April, 1991)

  A C Chandley
• Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting. (1 April, 1991)

  R M Ridley, C D Frith, L A Farrer, P M Conneally
• Fabry disease in a large Nova Scotia kindred: carrier detection using leucocyte alpha-galactosidase activity and an NcoI polymorphism detected by an alpha-galactosidase cDNA clone. (1 April, 1991)

  A J Kirkilionis, D C Riddell, M W Spence, R G Fenwick
• Aldolase B mutations in Italian families affected by hereditary fructose intolerance. (1 April, 1991)

  G Sebastio, R de Franchis, P Strisciuglio, G Andria, C Dionisi Vici, G Sabetta, R Gatti, N C Cross, T M Cox
• Molecular heterogeneity at the phenylalanine hydroxylase locus in the population of the south-west of England. (1 April, 1991)

  L A Tyfield, M J Osborn, J B Holton
• Genetic analysis in cystic fibrosis using the amplification refractory mutation system (ARMS): the J3.11 MspI polymorphism. (1 April, 1991)

  C R Newton, C Summers, L E Heptinstall, J R Lynch, R S Finniear, D Ogilvie, J C Smith, A F Markham
• Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene. (1 April, 1991)

  M Losekoot, R Fodde, C L Harteveld, H van Heeren, P C Giordano, L N Went, L F Bernini
• Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome. (1 April, 1991)

  O W Quarrell, R G Snell, M A Curtis, S H Roberts, P S Harper, D J Shaw
• PCR amplification of genomic DNA from a 24 year old lysate derived from washed human erythrocytes. (1 April, 1991)

  W R Chegwidden, P J Venta, R E Tashian
• Hereditary multiple exostoses. (1 April, 1991)

  R C Hennekam
• Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiency. (1 April, 1991)

  I M Buntinx, P J Willems, S E Spitaels, P J Van Reempst, A M De Paepe, J E Dumon
• Cardiac rhabdomyomata and megacystis-microcolon-intestinal hypoperistalsis syndrome. (1 April, 1991)

  R T Couper, R W Byard, E Cutz, D A Stringer, P R Durie
• Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance. (1 April, 1991)

  J C de Almeida, D F Reis, J Llerena Júnior, J Barbosa Neto, R L Pontes, S Middleton, L F Telles
• Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalities. (1 April, 1991)

  C P Bennett, D R Betts, M J Seller
• Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1). (1 April, 1991)

  J P Park, J B Moeschler, S Z Berg, D H Wurster-Hill
• Reproductive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimates. (1 April, 1991)

  M R Passos-Bueno, M Zatz