Subchromosomal localization of a gene (XRCC5) involved in double strand break repair to the region 2q34-36 M. HafezparastG. P. KaurP. A. Jeggo OriginalPaper Pages: 413 - 421
Caffeine enhanced measurement of mutagenesis by low levels of γ-irradiation in human lymphocytes Theodore T. PuckHelvise MorseCharles A. Waldren OriginalPaper Pages: 423 - 429
Genetic diversity of mitomycin C-hypersensitive Chinese hamster cell mutants: A new complementation group with chromosomal instability W. J. I. OverkampM. A. RooimansM. Z. Zdzienicka OriginalPaper Pages: 431 - 437
Adenovirus-mediated correction of the genetic defect in hepatocytes from patients with familial hypercholesterolemia Karen KozarskyMariann GrossmanJames M. Wilson OriginalPaper Pages: 449 - 458
Complementation analysis of Chediak-Higashi Syndrome: The same gene may be responsible for the defect in all patients and species Charles M. PerouJerry Kaplan OriginalPaper Pages: 459 - 468
The use of methylthioadenosine phosphorylase activity to select for human chromosome 9 in interspecies and intraspecies hybrid cells Bruce W. PorterfieldHelen PomykalaManuel O. Diaz OriginalPaper Pages: 469 - 477
The effectiveness of restriction endonucleases in cell killing and mutation Nina D. CostaWalter K. MassonJohn Thacker OriginalPaper Pages: 479 - 490
Hepatic gene therapy: Efficient retroviral-mediated gene transfer into rat hepatocytes in vivo Tadeusz M. KolodkaMilton FinegoldSavio L. C. Woo OriginalPaper Pages: 491 - 497
Chromosomal localization and cDNA sequence of human BTEB, a GC box binding protein Norihisa OheYuichi YamasakiYoshiaki Fujii-Kuriyama Brief Communication Pages: 499 - 503
The gene for the iron sulfur protein of succinate dehydrogenase (SDH-IP) maps to human chromosome 1p35-36.1 Susanne LeckschatDeena Ream-RobinsonImmo E. Scheffler Brief Communication Pages: 505 - 511