| Higher-primate phylogeny--why can't we decide? | R Holmquist, MM Miyamoto, M Goodman | 201 |
| Analysis of higher-primate phylogeny from transversion differences in nuclear and mitochondrial DNA by Lake's methods of evolutionary parsimony and operator metrics | R Holmquist, MM Miyamoto, M Goodman | 217 |
| Molecular evolution of the human immunodeficiency and related viruses | S Yokoyama, L Chung, T Gojobori | 237 |
| Molecular characteristics of diverse populations are consistent with the hypothesis of a recent invasion of Drosophila melanogaster by mobile P elements | D Anxolabehere, MG Kidwell, G Periquet | 252 |
| Phylogenetic relationships among Japanese, rhesus, Formosan, and crab- eating monkeys, inferred from restriction-enzyme analysis of mitochondrial DNAs | K Hayasaka, S Horai, T Gojobori, T Shotake, K Nozawa | 270 |
| The phylogenetic origin of the bifunctional tyrosine-pathway protein in the enteric lineage of bacteria | S Ahmad, RA Jensen | 282 |
| Relative efficiencies of the maximum parsimony and distance-matrix methods in obtaining the correct phylogenetic tree | J Sourdis, M Nei | 298 |
