Table of contents

Research Article

• The association of Angelman's syndrome with deletions within 15q11-13. (1 February, 1989)

  M Pembrey, S J Fennell, J van den Berghe, M Fitchett, D Summers, L Butler, C Clarke, M Griffiths, E Thompson, M Super
• Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis. (1 February, 1989)

  A Figus, R Lampis, M Devoto, M S Ristaldi, A Ideo, S de Virgilis, A M Nurchi, A Corrias, R Corda, M E Lai
• Prenatal exclusion testing for Huntington's disease: a problem of too much information. (1 February, 1989)

  F A Millan, A Curtis, M Mennie, S Holloway, M Boxer, M J Faed, J W Crawford, W A Liston, D J Brock
• Familial supravalvular aortic stenosis: a genetic study. (1 February, 1989)

  F Chiarella, F D Bricarelli, G Lupi, P Bellotti, S Domenicucci, C Vecchio
• Spondyloenchondrodysplasia. (1 February, 1989)

  H Menger, K Kruse, J Spranger
• Interstitial deletion of distal 13q associated with Hirschsprung's disease. (1 February, 1989)

  M A Lamont, M Fitchett, N R Dennis
• Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy? (1 February, 1989)

  E Boltshauser, W Lang, T Spillmann, E Hof
• Knowledge and perceptions of haemoglobinopathy carrier screening among general practitioners in Cardiff. (1 February, 1989)

  D Shickle, A May
• Rhodanese isozymes in three subjects with Leber's optic neuropathy. (1 February, 1989)

  D B Whitehouse, C J Poole, P R Kind, D A Hopkinson
• Joseph Adams (1756-1818). (1 February, 1989)

  A E Emery
• Stickler's syndrome. (1 February, 1989)

  I K Temple
• Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase. (1 February, 1989)

  I A Glass, C A Swindlehurst, D A Aitken, W McCrea, E Boyd
• A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation. (1 February, 1989)

  F S Yen, P E Podruch, B Weisskopf
• Familial distal trisomy 8(q24.13----qter). (1 February, 1989)

  D R Romain, R A Bloxham, L M Columbano-Green, C J Chapman, R G Parfitt, R H Smythe, H Cairney
• Is there an autosomal recessive form of the split hand and split foot malformation? (1 February, 1989)

  J Zlotogora, N Nubani