Table of contents

Research Article

• Genetic factors in amyloidosis. (1 December, 1975)

  P K Thomas
• Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio. (1 December, 1975)

  A Westwood, D N Raine
• Hirschsprung's disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly in sibs: a case for fetoscopy. (1 December, 1975)

  K M Laurence, R Prosser, I Rocker, J F Pearson, C Richard
• Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature. (1 December, 1975)

  C Sirinavin, A A Trowbridge
• Polydactyly and brachymetapody in two English families. (1 December, 1975)

  S B Holt
• X-linked mental retardation associated with macro-orchidism. (1 December, 1975)

  G Turner, C Eastman, J Casey, A McLeay, P Procopis, B Turner
• Genetics of the complement system. (1 December, 1975)

  P Lachmann
• Differences in human X isochromosomes. (1 December, 1975)

  J H Priest, R D Blackston, K S Au, S L Ray
• 45,X Turner's syndrome in monozygotic twin sisters. (1 December, 1975)

  G Pescia, P E Ferrier, D Wyss-Hutin, D Klein
• The Stickler syndrome presenting as a dominantly inherited cleft palate and blindness. (1 December, 1975)

  J G Hall, H Herrod
• Distal brachyphalangy of the thumb in mental retardation. (1 December, 1975)

  M M Villaverde, J A da Silva
• The search for relevant cell culture research in cystic fibrosis: one researcher's opinion. (1 December, 1975)

  B S Danes
• A family with an inherited translocation involving the no. 4/no. 21 chromosomes. (1 December, 1975)

  J M Darmady, M Seabright
• Trisomy of the short arm of chromosome 10. (1 December, 1975)

  Y Nakagome, H Kobayashi
• Autosomal recessive oculopharyngeal muscular dystrophy. (1 December, 1975)

  K Fried, A Arlozorov, R Spira
• Partial trisomy for the long arms of chromosome no. 5 due to insertion and further 'aneusomie de recombinaison'. (1 December, 1975)

  P Jalbert, H Jalbert, B Sele, C Mouriquand, J Malka, J Boucharlat, H Pison
• Bloom's syndrome: a probable new case with cytogenetic findings. (1 December, 1975)

  C A Bourgeois, M H Calverley, L Forman, P E Polani
• Trisomy 4q32 leads to 4qter due to a maternal 4/21 translocation. (1 December, 1975)

  C Baccichetti, R Tenconi, F Anglani, F Zacchello
• Letter: Mutation as the source of the abnormal gene for plasma cholinesterase. (1 December, 1975)

  N E Simpson