Table of contents

Research Article

• Molecular genetics of human chromosome 21. (1 May, 1987)

  P C Watkins, R E Tanzi, S V Cheng, J F Gusella
• Fryns syndrome: a variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasia. (1 May, 1987)

  J P Fryns
• Attitudes towards predictive testing in Huntington's disease: a recent survey in Belgium. (1 May, 1987)

  G Evers-Kiebooms, J J Cassiman, H van den Berghe
• Structural rearrangements in the parents of children with primary trisomy 21. (1 May, 1987)

  D A Couzin, J L Watt, G S Stephen
• Neuraminidase deficiency: case report and review of the phenotype. (1 May, 1987)

  I D Young, E P Young, J Mossman, A R Fielder, J R Moore
• Cleft lip and palate, pili torti, malformed ears, partial syndactyly of fingers and toes, and mental retardation: a new syndrome? (1 May, 1987)

  J Zlotogora, Y Zilberman, A Tenenbaum, M R Wexler
• Angelman (happy puppet) syndrome in a girl and her brother. (1 May, 1987)

  J A Fisher, J Burn, F W Alexander, D Gardner-Medwin
• Folate sensitive site at 10q23 and its expression as a deletion. (1 May, 1987)

  E L Maltby, S Higgins
• Partial trisomy 6q: case report with necropsy findings. (1 May, 1987)

  C J Franchino, D Beneck, M A Greco, S R Wolman
• Duplication 9p due to unequal sister chromatid exchange. (1 May, 1987)

  T Mattina, G Sorge, G Milone, R Garozzo, L Conti
• A case of de novo interstitial deletion 3q. (1 May, 1987)

  N Okada, T Hasegawa, M Osawa, Y Fukuyama
• Interstitial deletion and ring chromosome derived from 16q. (1 May, 1987)

  C M Krauss, D Caldwell, L Atkins