dc.creator | Hayakawa, Takao | en |
dc.date.accessioned | 2011-07-12T18:38:51Z | en |
dc.date.available | 2011-07-12T18:38:51Z | en |
dc.date.created | 1987 | en |
dc.date.issued | 1987 | en |
dc.identifier.bibliographicCitation | Progress in Clinical and Biological Research 1987; 235: 15-29 | en |
dc.identifier.uri | http://hdl.handle.net/10822/540454 | en |
dc.format | Article | en |
dc.language | eng | en |
dc.source | 70289 | en |
dc.subject | DNA | en |
dc.subject | Drugs | en |
dc.subject | Government | en |
dc.subject | Technology | en |
dc.subject.classification | Drugs and Drug Industry | en |
dc.subject.classification | Biohazards of Genetic Research | en |
dc.title | Some Aspects of the Preclinical Safety of Drugs Produced by Recombinant DNA Technology: Japanese Government Regulatory Position | en |
dc.provenance | Digital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National Human Genome Research Institute | en |
dc.provenance | Digital citation migrated from OpenText Livelink Discovery Server database named GenETHX to DSpace collection GenETHX hosted by Georgetown University | en |