Table of contents

Research Article

• Feasibility of neonatal screening for Duchenne muscular dystrophy. (1 February, 1982)

  R Skinner, A E Emery, G Scheuerbrandt, J Syme
• Effect of exercise on serum creatine kinase in carriers of Duchenne muscular dystrophy. (1 February, 1982)

  R F Gaines, S M Pueschel, E A Sassaman, J L Driscoll
• An epidemiological and genetic study of facial clefting in France. I. Epidemiology and frequency in relatives. (1 February, 1982)

  C Bonaiti, M L Briard, J Feingold, B Pavy, J Psaume, G Migne-Tufferaud, J Kaplan
• Survivors of neuroblastoma and ganglioneuroma and their families. (1 February, 1982)

  S Bundey, K Evans
• Apnoea following suxamethonium: the genetic study of four generations of a family. (1 February, 1982)

  A A Morgan
• Genetic aspects of fibrodysplasia ossificans progressiva. (1 February, 1982)

  J M Connor, D A Evans
• Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation. (1 February, 1982)

  G C Webb, J L Halliday, D B Pitt, C G Judge, M Leversha
• Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly. (1 February, 1982)

  M J Faed, M A Lamont, K Baxby
• Chromosome distribution studies in XXY karyotypes. (1 February, 1982)

  M Kirsch-Volders, L Hens, H van den Berghe, B Scholberg, C Susanne
• De novo interstitial deletion in the long arm of chromosome 9: a new chromosome syndrome. (1 February, 1982)

  K L Ying, C J Curry, K B Rajani, S H Kassel, R S Sparkes
• A second patient with partial deletion of the short arm of chromosome 3: karyotype 46,XY,del(3)(p25). (1 February, 1982)

  M C Higginbottom, J T Mascarello, H Hassin, W K McCord
• A severely retarded male with deletion of chromosomes 15 (pter leads to q13) and 10 (q 26 leads to qter). (1 February, 1982)

  A Smith, G den Dulk
• Alobar holoprosencephaly and otocephaly in a female infant with a normal karyotype and placental villitis. (1 February, 1982)

  A R Gaba, G J Anderson, D L VanDyke, J L Chason