Table of contents

Research Article

• The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p. (1 October, 1992)

  L A Brueton, L van Herwerden, K A Chotai, R M Winter
• Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphism. (1 October, 1992)

  L M Kayes, V M Riccardi, W Burke, R L Bennett, K Stephens
• Screening and genetic counselling for relatives of patients with breast cancer in a family cancer clinic. (1 October, 1992)

  R S Houlston, L Lemoine, E McCarter, S Harrington, K MacDermot, J Hinton, L Berger, J Slack
• Sex ratios of affected and transmitting members of multiple case families with neural tube defects. (1 October, 1992)

  E C Mariman, B C Hamel
• A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man. (1 October, 1992)

  J A Crolla, N R Dennis, P A Jacobs
• Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13q. (1 October, 1992)

  C A Brandt, J M Hertz, M B Petersen, F Vogel, H Noer, M Mikkelsen
• Extravillus dividing fetal cells at CVS: evidence of their erythroblastic origin. (1 October, 1992)

  G Terzoli, R Cartolano, F Rossella, A Cantù-Rajnoldi, B Brambati, M Fraccaro, G Simoni
• The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24). (1 October, 1992)

  M Le Merrer, K Ben Othmane, V Stanescu, S Lyonnet, L Van Maldergem, G Royer, A Munnich, P Maroteaux
• Recognition of thalidomide defects. (1 October, 1992)

  R W Smithells, C G Newman
• Postgraduate teaching in clinical genetics in the United Kingdom. (1 October, 1992)

  A W Johnston
• Difficult diagnosis of the fragile X syndrome made possible by direct detection of DNA mutations. (1 October, 1992)

  J Tarleton, S Wong, D Heitz, C Schwartz
• The OEIS complex (omphalocele-exstrophy-imperforate anus-spinal defects): recurrence in sibs. (1 October, 1992)

  N M Smith, H M Chambers, M E Furness, E A Haan
• Lethal olivopontoneocerebellar hypoplasia with dysmorphic features in sibs. (1 October, 1992)

  I D Young, P A McKeever, M V Squier, J Grant
• A new X linked syndrome with mental retardation and craniofacial dysmorphism? (1 October, 1992)

  I Hyde-Forster, G McCarthy, A C Berry
• Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent. (1 October, 1992)

  C J Van Der Burgt, G F Merkx, A H Janssen, J C Mulder, R F Suijkerbuijk, D F Smeets
• A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line. (1 October, 1992)

  L R Willatt, B C Davison, D Goudie, J Alexander, H M Dyson, P E Jenks, M E Ferguson-Smith
• Trisomy 15 mosaicism in an IVF fetus. (1 October, 1992)

  C P Bennett, T Davis, M J Seller
• De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome. (1 October, 1992)

  L Telvi, J M Pinard, R Ion, P M Sinet, A Nicole, J Feingold, O Dulac, A Pompidou, G Ponsot
• Premature chromosome condensation in a child with trisomy 21. (1 October, 1992)

  K Prabhakara, B Kar, S K Murthy
• Familial postaxial acrofacial dysostosis syndrome. (1 October, 1992)

  A Giannotti, M C Digilio, Q Virgili, M G Obregon, A M Guadagni, T Ventura, B Dallapiccola
• Report of ENMC workshop on the limb-girdle muscular dystrophies. (1 October, 1992)

  A Clarke
• Patent ductus arteriosus in four generations of a family. (1 October, 1992)

  J C Rogers, M L Begleiter, D J Harris
• Linkage disequilibrium between D16S94 and the locus for adult polycystic kidney disease (PKD1) (1 October, 1992)

  R G Elles