Table of contents

Research Article

• Genetic and clinical patterns of heritable cerebellar ataxias in adults. I. Genetic analyses. (1 December, 1980)

  K Kondo, I Sobue
• Autosomal recessive peripheral sensory neuropathy in 3 non-Ashkenazi Jewish families. (1 December, 1980)

  I Tamari, R M Goodman, I Sarova, M Hertz, R Adar, T Zvibach
• The Cohen syndrome: clinical and endocrinological studies of two new cases. (1 December, 1980)

  P Balestrazzi, L Corrini, G Villani, M P Bolla, F Casa, S Bernasconi
• Down syndrome and maternal age in South Glamorgan. (1 December, 1980)

  I D Young, E M Williams, R G Newcombe
• X;Y translocation in an adolescent mentally normal phenotypic male with features of hypogonadism. (1 December, 1980)

  R Bernstein, M R Pinto, M Almeida, S M Solarsh, J Meck, T Jenkins
• A familial polymorphic variant of chromosome 5. (1 December, 1980)

  M Seabright, N M Gregson, M Johnson
• Location of the gene for 21-hydroxylase deficiency. (1 December, 1980)

  V Pucholt, J S Fitzsimmons, K Gelsthorpe, M A Reynolds, R D Milner
• Selective IgA deficiency with 18q+ and 18q-- karyotypic anomalies. (1 December, 1980)

  R M Lewkonia, C C Lin, R H Haslam
• Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations. (1 December, 1980)

  M Ferraro, A De Capoa, C Mostacci, F Pelliccia, P Zulli, M A Baldini, Q Di Nisio
• A family segregating for E1j and E1k at cholinesterase locus 1. (1 December, 1980)

  R T Evans, J Iqbal, A A Dietz, T Lubrano, H M Rubinstein
• Sequential staining of euchromatic and heterochromatic regions of the human Y chromosome. (1 December, 1980)

  V J Goyanes
• A cryopreservative procedure for storing cultivated and uncultivated amniotic fluid cells in liquid nitrogen. (1 December, 1980)

  S Pentz, H Hörler
• Agenesis of the lung associated with a chromosome abnormality (46,XX,2p+). (1 December, 1980)

  B Say, N J Carpenter, G Giacoia, S Jegathesan
• A probable case of the homozygous condition of the aniridia gene. (1 December, 1980)

  S V Hodgson, K E Saunders
• Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype. (1 December, 1980)

  B M Lippe, R S Sparkes, B Fass, L Neidengard
• Interstitial deletion in the long arms of chromosome 1: 46,XY,del(1)(pter leads to q22::q25 leads to qter). (1 December, 1980)

  C E de Pablo, J M García Sagredo, M T Ferro, P Ferrando, C San Román
• Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15). (1 December, 1980)

  C Stoll, J Levy, M P Roth
• Neurological and neuropathological findings in ring chromosome 4. (1 December, 1980)

  R S Young, E L Zalneraitis
• Higher risk to D;G translocation carriers fo tdic(13;21) as compared to tdic(14;21) (1 December, 1980)

  A Daniel, K Williams, P R Lam-Po-Tang
• Cause of neural tube defects. (1 December, 1980)

  M J Seller