Table of contents

Research Article

• An exclusion map of Marfan syndrome. (1 February, 1990)

  S H Blanton, M Sarfarazi, H Eiberg, J de Groote, P A Farndon, M W Kilpatrick, A H Child, F M Pope, L Peltonen, C A Francomano
• Linkage analysis of five fibrillar collagen loci in a large French Marfan syndrome family. (1 February, 1990)

  C Boileau, G Jondeau, C Bonaiti, M Coulon, G Delorme, O Dubourg, J P Bourdarias, C Junien
• Linkage data for Marfan syndrome and markers on chromosomes 1 and 11. (1 February, 1990)

  J de Groote, P A Farndon, M V Kilpatrick, A de Paepe, J W Oorthuys, N C Nevin, A H Child, F M Pope
• Linkage analysis in Marfan syndrome. (1 February, 1990)

  R C Schwartz, S H Blanton, C A Hyde, T R Sottile, L Hudgins, M Sarfarazi, P Tsipouras
• Exclusion of COL2A1 as a candidate gene in a family with Wagner-Stickler syndrome. (1 February, 1990)

  A E Fryer, M Upadhyaya, M Littler, P Bacon, D Watkins, P Tsipouras, P S Harper
• Cardiovascular studies in the mucopolysaccharidoses. (1 February, 1990)

  J Nelson, M D Shields, H C Mulholland
• Carrier estimations in Duchenne muscular dystrophy families in Northern Ireland using RFLP analysis. (1 February, 1990)

  E D Kelly, C A Graham, A J Hill, N C Nevin
• Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus. (1 February, 1990)

  I Kondo, H Ohta, M Yazaki, J E Ikeda, J F Gusella, I Kanazawa
• Three cases of partial trisomy 7q owing to rare structural rearrangements of chromosome 7. (1 February, 1990)

  D R Romain, H Cairney, D Stewart, L M Columbano-Green, M Garry, M I Parslow, R Parfitt, R H Smythe, C J Chapman
• Yunis-Varon syndrome with severe osteodysplasty. (1 February, 1990)

  C Garrett, A C Berry, R H Simpson, C M Hall
• Moebius syndrome. (1 February, 1990)

  D Kumar
• A familial syndrome of microcephaly, sparse hair, mental retardation, and seizures. (1 February, 1990)

  A van Haeringen, J A Hurst, R Savidge, M Baraitser
• Neuroblastoma in a patient with Sotos' syndrome. (1 February, 1990)

  M A Nance, J P Neglia, D Talwar, S A Berry
• Compound heterozygosity for abetalipoproteinaemia and familial hypobetalipoproteinaemia. (1 February, 1990)

  S Keidar, A Etzioni, J G Brook, R Gershoni-Baruch, M Aviram
• Inverted tandem duplication of 8p12----p23.1 in a child with increased activity of glutathione reductase. (1 February, 1990)

  N C Nevin, P J Morrison, J Jones, M M Reid
• An apparent de novo terminal deletion of chromosome 2 (pter----p24:). (1 February, 1990)

  G L Francis, D B Flannery, J R Byrd, S T Fisher
• A workshop on Marfan syndrome, 10 June 1989, Farmington, CT, USA. (1 February, 1990)

  P Tsipouras
• Angelman's syndrome, abnormality of 15q11-13, and imprinting. (1 February, 1990)

  J G Hall
• Unilateral disomy as a possible explanation for Russell-Silver syndrome. (1 February, 1990)

  J G Hall