LEADER 02360nam 2200661 a 450 001 9910454615803321 005 20200520144314.0 010 $a1-281-11009-4 010 $a9786611110093 010 $a0-309-10868-3 035 $a(CKB)1000000000714189 035 $a(SSID)ssj0000277347 035 $a(PQKBManifestationID)12097785 035 $a(PQKBTitleCode)TC0000277347 035 $a(PQKBWorkID)10240486 035 $a(PQKB)10078188 035 $a(MiAaPQ)EBC3564137 035 $a(Au-PeEL)EBL3564137 035 $a(CaPaEBR)ebr10203750 035 $a(CaONFJC)MIL111009 035 $a(OCoLC)567909218 035 $a(EXLCZ)991000000000714189 100 $a20081021d2008 uy 0 101 0 $aeng 135 $aurcn||||||||| 181 $ctxt 182 $cc 183 $acr 200 10$aBiosocial surveys$b[electronic resource] /$fCommittee on Advances in Collecting and Utilizing Biological Indicators and Genetic Information in Social Science Surveys ; Maxine Weinstein, James W. Vaupel, and Kenneth W. Wachter, editors ; Committee on Population, Division of Behavioral and Social Sciences and Education, National Research Council of the National Academies 210 $aWashington, D.C. $cNational Academies Press$d2008 215 $axiii, 414 p. $cill 300 $aBibliographic Level Mode of Issuance: Monograph 311 $a0-309-10867-5 320 $aIncludes bibliographical references. 327 $apt. 1. What we've learned so far -- pt. 2. The potential and pitfalls of genetic information -- pt. 3. New ways of collecting, applying, and thinking about data. 606 $aSocial medicine 606 $aMedical ethics 606 $aBioethics 606 $aMedical genetics 606 $aDemography 608 $aElectronic books. 615 0$aSocial medicine. 615 0$aMedical ethics. 615 0$aBioethics. 615 0$aMedical genetics. 615 0$aDemography. 676 $a362.1 701 $aWeinstein$b Maxine$0949775 701 $aVaupel$b James W$0107134 701 $aWachter$b Kenneth W$0253847 712 02$aNational Research Council (U.S.).$bCommittee on Population, 2006-2007. 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910454615803321 996 $aBiosocial surveys$92146818 997 $aUNINA