Scientific Advances and Social Risks: Historical Perspectives of Genetic Screening Programs for Sickle Cell Disease, Tay-Sachs Disease, Neural Tube Defects, and Down Syndrome, 1970-1997
dc.contributor.author | Markel, Howard | |
dc.date.accessioned | 2011-08-10T13:55:42Z | |
dc.date.available | 2011-08-10T13:55:42Z | |
dc.date.issued | 1997 | |
dc.identifier.uri | https://hdl.handle.net/2027.42/85441 | |
dc.language.iso | en_US | en_US |
dc.publisher | NIH-DOE Working Group on Ethical, Legal and Social Implications of Human Genome Research | en_US |
dc.title | Scientific Advances and Social Risks: Historical Perspectives of Genetic Screening Programs for Sickle Cell Disease, Tay-Sachs Disease, Neural Tube Defects, and Down Syndrome, 1970-1997 | en_US |
dc.type | Book Chapter | en_US |
dc.subject.hlbsecondlevel | Medicine (General) | |
dc.subject.hlbtoplevel | Health Sciences | |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | History of Medicine, The Center for | en_US |
dc.contributor.affiliationum | University of Michigan Medical School | en_US |
dc.contributor.affiliationumcampus | Ann Arbor | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/85441/1/APPENDIX 6.pdf | |
dc.identifier.source | Promoting Safe and Effective Genetic Testing in the United States. Final Report of the Task Force on Genetic Screening. | en_US |
dc.owningcollname | History of Medicine, The Center for the |
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