Books on the topic 'Genetic screening – Psychological aspects'

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1

Fischer, Michael W., and Markus Hengstschläger. Genetic screening. Frankfurt am Main: Peter Lang, 2009.

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2

Sommer, Annemarie. Birth defects and genetic screening and counseling. Washington, D.C: Veterans Administration Central Office, Dept. of Medicine and Surgery, Agent Orange Projects Office, 1985.

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3

Sommer, Annemarie. Birth defects and genetic screening and counseling. Washington, D.C: Veterans Administration Central Office, Dept. of Medicine and Surgery, Agent Orange Projects Office, 1985.

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4

Juth, Niklas. Genetic information values and rights: The morality of presymptomatic genetic testing. Göteburg: Acta Universitatis Gothoburgensis, 2005.

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5

Presurgical psychological screening: Understanding patients, improving outcomes. Washington, DC: American Psychological Association, 2013.

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6

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

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7

What we have: A memoir. New York: Gotham Books, 2010.

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8

1942-, Taylor Robert L., ed. Distinguishing psychological from organic disorders: Screening for psychological masquerade. New York: Springer Pub. Co., 1990.

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9

Dierickx, Kris. Genetisch gezond?: Ethische en sociale aspecten van genetische tests en screenings. Antwerpen: Intersentia, 1999.

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10

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

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11

Gould, Randi L. Cancer and genetics: Answering your patients' questions. Huntington, NY: PRR, 1997.

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12

G, Resta Robert, ed. Psyche and helix: Psychological aspects of genetic counseling : essays. New York: Wiley-Liss, 2000.

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13

Fletcher, Joseph. The ethics of genetic control: Ending reproductive roulette : artificial insemination, surrogate pregnancy, nonsexual reproduction, genetic control and screening. Buffalo: Prometheus, 1988.

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14

Screening the past: Memory and nostalgia in cinema. New York: Routledge, 2004.

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15

Synchronicity and reunion: The genetic connection of adoptees and birthparents. Hobe Sound, Fla: FEA Pub., 1992.

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16

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

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17

Cook, Pam. Screening the past: Memory and nostalgia in cinema. London: Routledge, 2004.

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18

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

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19

Haker, Hille. Ethik der genetischen Frühdiagnostik: Sozialethische Reflexionen zur Verantwortung am Beginn des menschlichen Lebens. Paderborn: Mentis, 2002.

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20

Offit, Kenneth. Clinical cancer genetics: Risk counseling and management. New York: Wiley-Liss, 1998.

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21

Counseling about cancer: Strategies for genetic counseling. 2nd ed. New York: Wiley-Liss, 2002.

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22

Schneider, Katherine A. Counseling about cancer: Strategies for genetic counselors. 2nd ed. New York: Wiley-Liss, 2002.

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23

Schneider, Katherine A. Counseling about cancer: Strategies for genetic counselors. Dennisport, Mass: Graphic Illusions, 1994.

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24

The Cause of wars and aggression. Point Roberts, WA: Global Justice Pub., 2004.

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25

Filter, Bo. The cause of wars and aggression. Point Roberts, Wash: Global Justice Pub., 2004.

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26

1956-, Sarangi Srikant, and Clarke Angus 1954-, eds. Genetic testing: Accounts of autonomy, responsibility, and blame. Abingdon, Oxon: Routledge, 2011.

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27

Genetic privacy: A challenge to medico-legal norms. Cambridge, U.K: Cambridge University Press, 2002.

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28

Zakharov, I. A. GenEtika, ili, Rozhatʹ, nelʹzi︠a︡ klonirovatʹ. Novosibirsk: Izd-vo SO RAN, 2003.

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29

Kollek, Regine. Der medizinische Blick in die Zukunft: Gesellschaftliche Implikationen prädiktiver Gentests. Frankfurt am Main: Campus, 2008.

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30

Presurgical psychological screening in chronic pain syndromes: A guide for the behavioral health practitioner. Mahwah, N.J: L. Erlbaum Associates, 1996.

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31

United States. Congress. Senate. Committee on Commerce, Science, and Transportation. Subcommittee on Science, Technology, and Space. Prenatal genetic testing technology: Science, policy, and ethics : hearing before the Subcommittee on Science, Technology, and Space of the Committee on Commerce, Science, and Transportation, United States Senate, One Hundred Eighth Congress, first session, November 17, 2004. Washington: U.S. Government Printing Office, 2013.

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32

Marcel, Melançon, ed. Dépistage et diagnostic génétiques: Aspects cliniques, juridiques, éthiques et sociaux. [Québec]: Presses de lU̕niversité Laval, 1999.

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33

Lee, Ellis. Theories of rape: Inquiries into the causes of sexual aggression. New York: Hemisphere Pub. Corp., 1989.

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34

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

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35

Louhiala, Pekka. Preventing intellectual disability: Ethical and clinical issues. Cambridge, UK: Cambridge University Press, 2004.

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36

Breast cancer genes and the gendering of knowledge: Science and citizenship in the cultural context of the "new" genetics. Basingstoke [England]: Palgrave Macmillan, 2007.

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37

Bellino, Raffaello Maria. Critica della ragione predittiva: L'etica tra scienza e nescienza. Bari: Levante, 2004.

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38

United States. Congress. House. Committee on Education and the Workforce. Subcommittee on Employer-Employee Relations. Genetic nondiscrimination: Implications for employers and employees : hearing before the Subcommittee on Employer-Employee Relations of the Committee on Education and the Workforce, House of Representatives, One Hundred Seventh Congress, first session, hearing held in Washington, DC, July 24, 2001. Washington: U.S. G.P.O., 2002.

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39

Torres, Mauro. El incesto y los genes: Las compulsiones, el más temible flagelo mental! Santafé de Bogotá: Tercer Mundo Editores, 1997.

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40

Psychological aspects of fetal screening and the new genetics. [U.K.]: Society for Reproductive and Infant Psychology, 1993.

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41

(Foreword), Francis S. Collins, ed. Genetic Testing For Cancer: Psychological Approaches for Helping Patients and Families. American Psychological Association (APA), 2004.

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42

(Editor), Suzanne M. Miller, Susan H. McDaniel (Editor), John S. Rolland (Editor), and Suzanne L. Feetham (Editor), eds. Individuals, Families, and the New Era of Genetics: Biopsychosocial Perspectives. W. W. Norton, 2006.

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43

1951-, Miller Suzanne M., ed. Individuals, families, and the new era of genetics: Biopsychosocial perspectives. New York: W.W. Norton, 2006.

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44

(Editor), Suzanne M. Miller, Susan H. McDaniel (Editor), John S. Rolland (Editor), and Suzanne L. Feetham (Editor), eds. Individuals, Families, and the New Era of Genetics: Biopsychosocial Perspectives. W. W. Norton, 2006.

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45

(Editor), Janna Thompson, and Loane Skene (Editor), eds. Ethics of Genetic Screening and Therapy. Cambridge University Press, 2008.

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46

United States. Congress. Office of Technology Assessment., ed. Genetic monitoring and screening in the workplace. Washington, DC: Congress of the U.S., Office of Technology Assessment, 1990.

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47

Sherman, Elias, and Simpson Joe Leigh 1943-, eds. Maternal serum screening for fetal genetic disorders. New York: Churchill Livingstone, 1992.

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48

1952-, Valverde Carlos, ed. Genetic screening of newborns: An ethical inquiry. Hauppauge, N.Y: Nova Science Publishers, 2009.

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49

America Debates Genetic DNA Testing (America Debates). Rosen Central, 2007.

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50

Na. Genetic Testing and Privacy. Privacy Commissioner of Canada, 1992.

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