Books on the topic 'Social chromosome'

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1

Bogdanov, I︠U︡ F. Sinaptonemnyĭ kompleks: Indikator dinamiki meĭoza i izmenchivosti khromosom. Moskva: Tov-vo nauch. izd. KMK, 2007.

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2

Risky business: Genetic testing and exclusionary practices in the hazardous workplace. Cambridge [England]: Cambridge University Press, 1991.

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3

Handbook of genomics and the family: Psychosocial context for children and adolescents. New York: Springer, 2010.

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4

Nelkin, Dorothy. Dangerous diagnostics: The social power of biological information. New York: Basic Books, 1989.

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5

F, Cranor Carl, ed. Are genes us?: The social consequences of the new genetics. New Brunswick, N.J: Rutgers University Press, 1994.

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6

Duster, Troy. Backdoor to eugenics. 2nd ed. New York, NY: Routledge, 2002.

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7

Duster, Troy. Backdoor to eugenics. New York: Routledge, 1990.

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8

Blood matters: A journey along the genetic frontier. London: Granta, 2009.

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9

Nelkin, Dorothy. Dangerous diagnostics: The social power of biological information : with a new preface. Chicago: University of Chicago Press, 1994.

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10

1923-, Kennet Wayland, Robinson Paul, and Association Descartes, eds. Parliaments and screening: A conference on the ethical and social problems arising from testing and screening for HIV and AIDS : the role of parliaments and the media : conference report and studies of the handling of bioethics in the twelve national parliaments of the European Union. London: John Libbey, 1995.

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11

Sack, George. USMLE Road Map. New York: McGraw-Hill, 2008.

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12

Canada. Privacy Commissioner of Canada. Genetic testing and privacy. Ottawa, Ont: Privacy Commissioner of Canada, 1992.

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13

Future perfect: Confronting decisions about genetics. New York: Columbia University Press, 2001.

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14

Mara, Buchbinder, ed. Saving babies?: The consequences of newborn genetic screening. Chicago: The University of Chicago Press, 2013.

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15

Wieser, Bernhard. Assessing life: On the organisation of genetic testing. München: Profil, 2010.

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16

Pennisi, Silvia. Consulenza e test genetici nella pratica clinica: Aspetti etici, giuridici e sociali. Padova: Il poligrafo, 2012.

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17

Community genetics and genetic alliances: Eugenics, carrier testing, and networks of risk. Abingdon, Oxon: Routledge, 2009.

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18

As the future catches you: How genomics & other forces are changing your work, health & wealth. New York: Crown Business, 2001.

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19

Enriquez, Juan. As the Future Catches You. New York: Crown Publishing Group, 2001.

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20

Enriquez, Juan. Mientras el futuro te alcanza: Cómo la genómica y otras tecnologías están cambiando tu vida, trabajo, salud y riqueza. México, D.F: Grijalbo, 2005.

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21

Negotiating risk: British Pakistani experiences of genetics. New York: Berghahn Books, 2009.

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22

Bear, Greg. Darwin's children. New York: Ballantine Books, 2003.

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23

Bear, Greg. Darwin's children. New York, NY: Ballantine, 2003.

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24

Bear, Greg. Darwin's children. London: HarperCollins, 2003.

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25

Bear, Greg. Darwin's children. New York: Ballantine, 2003.

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26

Bear, Greg. Darwin's children. London: HarperCollins, 2004.

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27

Bear, Greg. Les enfants de Darwin. Paris: Librairie générale française, 2007.

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28

Bear, Greg. Darwin's Children. New York: Random House Publishing Group, 2003.

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29

Sulston, John. The common thread: A story of science, politics, ethics, and the human genome. London: New York, 2002.

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30

The genome incorporated: Constructing biodigital identity. Burlington, VT: Ashgate Pub., 2010.

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31

The sociology of medical screening: Critical perspectives, new directions. 2nd ed. Chichester, West Sussex, U.K: Wiley-Blackwell, 2013.

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32

Katie, Featherstone, ed. Risky relations: Family, kinship and the new genetics. New York: Berg, 2006.

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33

Rabinow, Paul. A machine to make a future: Biotech chronicles. Princeton, NJ: Princeton University Press, 2005.

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34

Nauchnye shkoly v otechestvennoĭ biologii XX veka i ikh transformat︠s︡ii︠a︡ v uslovii︠a︡kh sot︠s︡iokulʹturnykh izmeneniĭ. Moskva: Tovarishchestvo nauchnykh izdaniĭ KMK, 2007.

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35

Palermo, Gianpiero D., and E. Scott Sills. Human Embryos and Preimplantation Genetic Technologies: Ethical, Social, and Public Policy Aspects. Elsevier Science & Technology Books, 2019.

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36

Sills, E. Scott, and Gianpiero Palermo. Human Embryos and Preimplantation Genetic Technologies: Ethical, Social, and Public Policy Aspects. Elsevier Science & Technology, 2019.

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37

Betta, Michela. Moral, Social, and Commercial Imperatives of Genetic Testing and Screening: The Australian Case. Springer Netherlands, 2010.

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38

Betta, Michela. Moral, Social, and Commercial Imperatives of Genetic Testing and Screening: The Australian Case. Springer, 2007.

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39

Charbonneau, Jan, and Christine Critchley. Direct-To-Consumer Genetic Testing: A Guide to the Practical, Ethical, Legal, and Social Issues. Elsevier Science & Technology Books, 2019.

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40

Frameworks of Choice: Predictive and Genetic Testing in Asia. Amsterdam University Press, 2010.

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41

Sleeboom-Faulkner, Margaret. Frameworks of Choice: Predictive and Genetic Testing in Asia. Amsterdam University Press, 2010.

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42

Sleeboom-Faulkner, Margaret. Frameworks of Choice: Predictive and Genetic Testing in Asia. Amsterdam University Press, 2010.

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43

Betta, Michela. The Moral, Social, and Commercial Imperatives of Genetic Testing and Screening: The Australian Case (International Library of Ethics, Law, and the New Medicine). Springer, 2006.

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44

Konrad, Monica. Narrating the New Predictive Genetics: Ethics, Ethnography and Science (Cambridge Studies in Society and the Life Sciences). Cambridge University Press, 2005.

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45

Konrad, Monica. Narrating the New Predictive Genetics: Ethics, Ethnography and Science (Cambridge Studies in Society and the Life Sciences). Cambridge University Press, 2005.

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46

Konrad, Monica. Narrating the New Predictive Genetics: Ethics, Ethnography and Science. Cambridge University Press, 2009.

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47

Konrad, Monica. Narrating the New Predictive Genetics: Ethics, Ethnography and Science. Cambridge University Press, 2011.

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48

(Editor), Stephen G. Post, and Peter J. Whitehouse (Editor), eds. Genetic Testing for Alzheimer Disease: Ethical and Clinical Issues. The Johns Hopkins University Press, 1998.

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49

1951-, Post Stephen Garrard, and Whitehouse Peter J, eds. Genetic testing for Alzheimer disease: Ethical and clinical issues. Baltimore: Johns Hopkins University Press, 1998.

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50

Duster, Troy. Backdoor to Eugenics. Taylor & Francis Group, 2004.

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