Table of contents

Research Article

• Erroneous theories of sex determination. (1 June, 1985)

  U Mittwoch
• An hypothesis regarding the origin of aneuploidy in man: indirect evidence from an experimental model. (1 June, 1985)

  M H Kaufman
• Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome. (1 June, 1985)

  C S Brown, P L Pearson, N S Thomas, M Sarfarazi, P S Harper, D J Shaw
• Polymorphism of DNA sequence in the human pro alpha 2(I) collagen gene. (1 June, 1985)

  A F Grobler-Rabie, D K Brebner, S Vandenplas, G Wallis, R Dalgleish, R E Kaufman, A J Bester, C G Mathew, C D Boyd
• Exclusion of the alpha 1(II) cartilage collagen gene as the mutant locus in type IA osteogenesis imperfecta. (1 June, 1985)

  B Sykes, R Smith, S Vipond, C Paterson, K Cheah, E Solomon
• Seckel syndrome: an overdiagnosed syndrome. (1 June, 1985)

  E Thompson, M Pembrey
• A new brachydactyly syndrome with similarities to Julia Bell types B and E. (1 June, 1985)

  P Pitt, I Williams
• Clinical and haematological evaluation of beta thalassaemia intermedia with increased Hb F and Hb A2 in heterozygotes: beta thalassaemia intermedia I. (1 June, 1985)

  C Altay, A Gurgey
• Clinical and haematological evaluation of beta thalassaemia intermedia characterised by unusually low Hb F and increased Hb A2: beta thalassaemia intermedia II. (1 June, 1985)

  A Gurgey, S Kayin, E Kansu, C Altay
• Extra Yq and partial monosomy 12p due to a Y;12 translocation in a boy with features of the 12p deletion syndrome. (1 June, 1985)

  E Orye, M Craen, G Laureys, R van Coster, B van Mele
• Interstitial deletion of the long arm of chromosome 11. (1 June, 1985)

  J M Klep-de Pater, H F de France, J B Bijlsma
• Interstitial deletion 2q24.3: case report with high resolution banding. (1 June, 1985)

  J Bernar, R S Sparkes, S Allensworth
• Hyperinsulinaemic hypoglycaemia in an infant with mosaic trisomy 13. (1 June, 1985)

  V S Smith, G P Giacoia
• Complex cardiac malformation in a case of trisomy 9. (1 June, 1985)

  T Williams, I Zardawi, R Quaife, I D Young
• Phenotypic delineation of ring chromosome 15 and Russell-Silver syndromes. (1 June, 1985)

  G N Wilson, S E Sauder, M Bush, I Z Beitins