Table of contents

Research Article

• Incidence of Duchenne muscular dystrophy in New South Wales and Australian Capital Territory. (1 August, 1980)

  J Cowan, J Macdessi, A Stark, G Morgan
• Pitfalls of genetic counselling in Pfeiffer's syndrome. (1 August, 1980)

  M Baraitser, M Bowen-Bravery, P Saldaña-Garcia
• Menkes X linked disease: heterozygous phenotype in uncloned fibroblast cultures. (1 August, 1980)

  N Horn
• Menkes X linked disease: two clonal cell populations in heterozygotes. (1 August, 1980)

  N Horn, P Mooy, V M McGuire
• Increase in the amount of fetal lymphocytes in maternal blood during pregnancy. (1 August, 1980)

  E L Assche, C Susanne
• Estimates of the likelihood that a Down's syndrome child of unknown genotype is a consequence of an inherited translocation. (1 August, 1980)

  S G Albright, E B Hook
• A family with diaphyseal aclasis and peripheral dysostosis. (1 August, 1980)

  A P Brooks, R Wynne-Davies
• Negro alpha-thalassaemia: genetic studies in homozygous sickle cell disease. (1 August, 1980)

  G R Serjeant, K P Mason, B E Serjeant
• Haemoglobin E trait and probable alpha-thalassaemia in a black American family: a family study. (1 August, 1980)

  A F El-Shirbiny, S Parkhurst, R E Bettigole, K D Tourbaf
• Recessively inherited growth hormone deficiency in a family from Iraq. (1 August, 1980)

  M D Donaldson, S M Tucker, D B Grant
• Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings. (1 August, 1980)

  R Bernstein, T Jenkins, B Dawson, J Wagner, G Dewald, G C Koo, S S Wachtel
• Dermatoglyphs in carriers of a balanced 15;21 translocation. (1 August, 1980)

  A Rodewald, M Zankl, H Zankl, K D Zang
• Segregation of an X ring chromosome in two generations. (1 August, 1980)

  B Dallapiccola, L Bruni, B Boscherini, A M Pasquino, L Chessa, P Vignetti
• Pericentric inversion (13) with two different recombinants in the same family. (1 August, 1980)

  E M Williamson, J F Miller, M Seabright
• Prenatal diagnosis of a de novo non-fluorescent Y chromosome. (1 August, 1980)

  J H Priest, A T Chen, P M Fernhoff, J A Reidy, C Whitsett
• 13q-/r(13) mosaicism. (1 August, 1980)

  N Niikawa, T Tamura, F Tomiyasu, T Kajii
• 45,X/46,XY/47,XY, +21 mosaicism in a hypogonadal phenotypic male. (1 August, 1980)

  M Sparagana, P W Wong, T R Dorsch, C Casten, M Rauer, K Szego
• Gonadal dysgenesis in a 46,XY female mosaic for double autosomal trisomies 8 and 21. (1 August, 1980)

  J M Sulewski, Thao-phuong-Dang, S Ward, R L Ladda
• Congenital horizontal gaze palsy and kyphoscoliosis. (1 August, 1980)

  E K Dretakis
• Classification of inherited brachydactylies. (1 August, 1980)

  H K Goswami, B D Chaurasia
• Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family. (1 August, 1980)

  G Morelli, C Mesolella, M L Cavaliere, M Stabile, V Ventruto
• Tuberous Sclerosis. (1 August, 1980)

  R A Pagon
• Congenital hypothyroidism and Klinefelter's syndrome. (1 August, 1980)

  F Harris