Table of contents

Research Article

• Muscular dystrophy in girls with X;autosome translocations. (1 December, 1986)

  Y Boyd, V Buckle, S Holt, E Munro, D Hunter, I Craig
• Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy. (1 December, 1986)

  V M Kean, H L Macleod, M W Thompson, P N Ray, C Verellen-Dumoulin, R G Worton
• Duchenne muscular dystrophy in one of monozygotic twin girls. (1 December, 1986)

  J Burn, S Povey, Y Boyd, E A Munro, L West, K Harper, D Thomas
• Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies. (1 December, 1986)

  A Clarke, S H Roberts, N S Thomas, A Whitfield, J Williams, P S Harper
• Molecular deletion analysis in Duchenne muscular dystrophy. (1 December, 1986)

  N S Thomas, P N Ray, R G Worton, P S Harper
• The screening of Duchenne muscular dystrophy patients for submicroscopic deletions. (1 December, 1986)

  K Hart, C Cole, A Walker, S Hodgson, L Johnson, V Dubowitz, P Ray, R Worton, M Bobrow
• The population genetics of Duchenne: natural and artificial selection in Duchenne muscular dystrophy. (1 December, 1986)

  J H Edwards
• Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families. (1 December, 1986)

  C J Bertelson, J A Bartley, A P Monaco, C Colletti-Feener, K Fischbeck, L M Kunkel
• Linkage studies in Duchenne and Becker muscular dystrophies. (1 December, 1986)

  A Walker, K Hart, C Cole, S Hodgson, L Johnson, V Dubowitz, M Bobrow
• Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy. (1 December, 1986)

  M W Thompson, P N Ray, B Belfall, C Duff, C Logan, I Oss, R G Worton
• Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis. (1 December, 1986)

  J M Old, K E Davies
• Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms. (1 December, 1986)

  M Lindlöf, H Kääriäinen, K E Davies, A de la Chapelle
• DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure. (1 December, 1986)

  E Bakker, E J Bonten, L F De Lange, H Veenema, D Majoor-Krakauer, M H Hofker, G J Van Ommen, P L Pearson
• A register based system for gene tracking in Duchenne muscular dystrophy. (1 December, 1986)

  A P Read, L Kerzin-Storrar, R C Mountford, R G Elles, R Harris
• Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene. (1 December, 1986)

  J R Yates, N A Affara, D M Jamieson, M A Ferguson-Smith, I Hausmanowa-Petrusewicz, J Zaremba, J Borkowska, A W Johnston, K Kelly
• X linked muscular dystrophy with contractures. (1 December, 1986)

  A W Johnston, E McKay
• Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome. (1 December, 1986)

  N S Thomas, H Williams, L J Elsas, L C Hopkins, M Sarfarazi, P S Harper