Comparison of point mutation rates in different species with human mutation rates P. Propping I. Point Mutations Pages: 43 - 48
Amino-acid sequences of different species as source of information about mutation mechanisms Walter M. Fitch I. Point Mutations Pages: 67 - 69
Evidence on the mechanism of spontaneous mutations from human haemoglobin variants and some other proteins F. Vogel I. Point Mutations Pages: 71 - 76
Ageing of human fibroblasts in culture: Studies on enzymes and mutation Robin Holliday I. Point Mutations Pages: 83 - 86
The spontaneous azaguanine-resistant mutants of diploid human fibroblasts Robert DeMarsKarsten R. Held I. Point Mutations Pages: 87 - 110
Frequency of spontaneous chromosome mutations in spermatogenesis of mice E. Schleiermacher II. Chromosome Mutations Pages: 115 - 118
Chromosomal aneuploidy in human spermatozoa I. H. PawlowitzkiP. L. Pearson II. Chromosome Mutations Pages: 119 - 122
Frequencies of spontaneous non-disjunction in metaphase II oocytes of mice G. Röhrborn II. Chromosome Mutations Pages: 123 - 125
Frequency of chromosome abnormalities in abortions I. H. Pawlowitzki II. Chromosome Mutations Pages: 131 - 136
Chromosome mutations: Frequency at birth in humans Patricia A. Jacobs II. Chromosome Mutations Pages: 137 - 140
The effect of maternal age on the incidence of Down's syndrome Margareta MikkelsenJ. Stene II. Chromosome Mutations Pages: 141 - 146
Satellite association. A possible cause of chromosome aberrations W. RosenkranzS. Holzer II. Chromosome Mutations Pages: 147 - 150
Spontaneous chromosome aberrations in human somatic cells N. P. Bochkov II. Chromosome Mutations Pages: 159 - 164
Diabetes mellitus in patients with aneuploid chromosome aberrations and in their parents Johannes Nielsen II. Chromosome Mutations Pages: 165 - 170
Immunological aberrations in patients with aneuploid chromosome abnormalities and in their parents Johannes Nielsen II. Chromosome Mutations Pages: 171 - 176