| Positive darwinian selection observed at the variable-region genes of immunoglobulins | T Tanaka, M Nei | 447 |
| The involucrin gene of the owl monkey: origin of the early region | H Tseng, H Green | 460 |
| The involucrin gene of the orangutan: generation of the late region as an evolutionary trend in the hominoids | P Djian, H Green | 469 |
| Concerted evolution of light satellite DNA in genus Mus implies amplification and homogenization of large blocks of repeats | B Dod, E Mottez, E Desmarais, F Bonhomme, G Roizes | 478 |
| Restriction-map variation with the yellow-achaete-scute region in five populations of Drosophila melanogaster | WF Eanes, J Labate, JW Ajioka | 492 |
| Evolution of ionic channels of biological membranes | F Franciolini, A Petris | 503 |
| Relative efficiencies of the Fitch-Margoliash, maximum-parsimony, maximum-likelihood, minimum-evolution, and neighbor-joining methods of phylogenetic tree construction in obtaining the correct tree | N Saitou, T Imanishi | 514 |
| Statistical tests for detecting gene conversion | S Sawyer | 526 |
| The statistical analysis of mitochondrial DNA polymorphisms: chi 2 and the problem of small samples | DA Roff, P Bentzen | 539 |
| A shift in the third-codon-position nucleotide frequency in alcohol dehydrogenase genes in the genus Drosophila | WT Starmer, DT Sullivan | 546 |
| Satellite DNA and higher-primate phylogeny | JC Fowler, JD Skinner, LA Burgoyne, RD Drinkwater | 553 |
