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DNA-Sequence Patenting: National Society of Genetic Counselors (NSGC) Position Paper

dc.contributor.authorYesley, Anneen_US
dc.contributor.authorMcIntosh, Nathalieen_US
dc.contributor.authorBraddock, Bonnie R.en_US
dc.contributor.authorBranda, Kelly J.en_US
dc.contributor.authorEanet, Karenen_US
dc.contributor.authorGoldberg, Simonen_US
dc.contributor.authorKieffer, Stephanie A.en_US
dc.contributor.authorPrimiano, Lisaen_US
dc.contributor.authorQuercia, Nadaen_US
dc.contributor.authorTaylor, Kelly A.en_US
dc.contributor.authorTsipis, Judithen_US
dc.contributor.authorYashar, Beverly M.en_US
dc.date.accessioned2006-09-11T15:26:35Z
dc.date.available2006-09-11T15:26:35Z
dc.date.issued2002-08en_US
dc.identifier.citationMcIntosh, Nathalie; Braddock, Bonnie R.; Branda, Kelly J.; Eanet, Karen; Goldberg, Simon; Kieffer, Stephanie A.; Primiano, Lisa; Quercia, Nada; Taylor, Kelly A.; Tsipis, Judith; Yashar, Beverly M.; Yesley, Anne; (2002). "DNA-Sequence Patenting: National Society of Genetic Counselors (NSGC) Position Paper." Journal of Genetic Counseling 11(4): 241-243. <http://hdl.handle.net/2027.42/44919>en_US
dc.identifier.issn1059-7700en_US
dc.identifier.issn1573-3599en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44919
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12735296&dopt=citationen_US
dc.description.abstractIn November 2000, the Genetic Services Committee of the National Society of Genetic Counselors (NSGC) convened a working group to draft a position paper on patenting of DNA-sequences. The mandate of the group was to produce general position statements that support the perspective and needs of consumers of DNA-based genetic tests and therapies (our patients and their families) and participants in DNA-based genetic research. After review and discussion of the literature on DNA-sequence patenting issues, the working group drafted position statement points that support current United States Patent and Trademark Office (USPTO) guidelines; broad licensing of DNA-sequence patents; nonenforcement of DNA-sequence patents in noncommercial research; reasonable royalty rates; an informed consent process for research participants that discloses whether they can share in any financial rewards relating to the project; the development of guidelines for licensing of DNA-sequence patents; and the establishment of oversight organizations to monitor licensing of DNA-sequence patents. These position statements were approved by the NSGC Board of Directors in the fall of 2001.en_US
dc.format.extent14269 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; National Society of Genetic Counselors, Inc. ; Springer Science+Business Mediaen_US
dc.subject.otherRoyaltiesen_US
dc.subject.otherGenetic Therapiesen_US
dc.subject.otherPosition Paperen_US
dc.subject.otherPublic Health/Gesundheitswesenen_US
dc.subject.otherPatentingen_US
dc.subject.otherEthicsen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherHuman Geneticsen_US
dc.subject.otherGynecologyen_US
dc.subject.otherClinical Psychologyen_US
dc.subject.otherDNA-sequenceen_US
dc.subject.otherLicensingen_US
dc.subject.otherGenetic Testingen_US
dc.subject.otherNational Society of Genetic Counselors (NSGC)en_US
dc.titleDNA-Sequence Patenting: National Society of Genetic Counselors (NSGC) Position Paperen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherGreater Baltimore Medical Center, Harvey Institute of Human Genetics, Baltimore, Marylanden_US
dc.contributor.affiliationotherDepartment of Biology, Brandeis University, Waltham, Massachusettsen_US
dc.contributor.affiliationotherClinical Genetics, University of Alberta Hospital, Edmonton, Canadaen_US
dc.contributor.affiliationotherDivision of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, Canadaen_US
dc.contributor.affiliationotherOffice of Technology Licensing, Stanford University, Palo Alto, Californiaen_US
dc.contributor.affiliationotherSection of Genetics, Upstate Medical University, Syracuse, New Yorken_US
dc.contributor.affiliationotherDepartment of Biology, Brandeis University, Waltham, Massachusettsen_US
dc.contributor.affiliationotherDana Farber Cancer Institute, Boston, Massachusettsen_US
dc.contributor.affiliationotherAmerican Medical Association, Chicago, Illinoisen_US
dc.contributor.affiliationotherDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennesseeen_US
dc.contributor.affiliationotherAthena Diagnostics, Inc., Worcester, Massachusettsen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid12735296en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44919/1/10897_2004_Article_375456.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/A:1016374314605en_US
dc.identifier.sourceJournal of Genetic Counselingen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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