000 01512nam a2200385Ia 4500
001 EBC461094
003 MiAaPQ
006 m o d |
007 cr cn|||||||||
008 090501s2009 enk sb 000 0 eng d
010 _z 2009018067
020 _z9780521509916 (hardback : alk. paper)
035 _a(MiAaPQ)EBC461094
035 _a(Au-PeEL)EBL461094
035 _a(CaPaEBR)ebr10349740
035 _a(CaONFJC)MIL233691
035 _a(OCoLC)609845622
040 _aMiAaPQ
_cMiAaPQ
_dMiAaPQ
050 4 _aRB155.65
_b.G68 2009
245 0 4 _aThe governance of genetic information
_h[electronic resource] :
_bwho decides? /
_cedited by Heather Widdows, Caroline Mullen.
260 _aCambridge ;
_aNew York :
_bCambridge University Press,
_c2009.
300 _axi, 235 p.
490 1 _aCambridge law, medicine, and ethics
504 _aIncludes bibliographical references.
533 _aElectronic reproduction. Ann Arbor, MI : ProQuest, 2015. Available via World Wide Web. Access may be limited to ProQuest affiliated libraries.
650 0 _aGenetic screening
_xMoral and ethical aspects.
650 0 _aGenetic screening
_xGovernment policy.
650 0 _aPrivacy, Right of.
650 0 _aMedical records
_xAccess control.
655 4 _aElectronic books.
700 1 _aWiddows, Heather,
_d1972-
700 1 _aMullen, Caroline.
710 2 _aProQuest (Firm)
830 0 _aCambridge law, medicine, and ethics.
856 4 0 _uhttp://ebookcentral.proquest.com/lib/aitie/detail.action?docID=461094
_zClick to View
999 _c123247
_d123247