1. Martin, G.M. (1978) Genetic syndromes in man with potential relevance to the pathobiology of aging. Birth Defects14, 5–39
2. Epstein, C.J., Martin, G.M., Schultz, A.L., and Motulsky, A.G. (1966) Werner's syndrome: a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process. Medicine45, 177–221
3. Goto, M., Miller, R.W., Ishikawa, Y., and Sugano, H. (1996) Excess of rare cancers in Werner syndrome (adult progeria). Cancer Epidemiol Biomarkers Prev.5, 239–246
4. Salk, D., Bryant, E., Hoehn, H., Johnston, P., and Martin, G.M. (1985) Growth characteristics of Werner syndrome cells in vitro. Adv. Exp. Med. Biol.190, 305–311
5. Fukuchi, K., Martin, G.M., and Monnat, R.J., Jr. (1989) Mutator phenotype of Werner syndrome is characterized by extensive deletions. Proc. Natl. Acad. Sci. USA86, 5893–5897