Books on the topic 'Genetic screening'
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Fischer, Michael W., and Markus Hengstschläger. Genetic screening. Frankfurt am Main: Peter Lang, 2009.
Bioethics, Nuffield Council on, ed. Genetic screening: Ethical issues. London: Nuffield Council on Bioethics, 1993.
Gregg, Anthony R., and Joe Leigh Simpson. Genetic screening and counseling. Philadelphia: W.B. Saunders Co., 2002.
Gregg, Anthony R., and Joe Leigh Simpson. Genetic screening and counseling. Philadelphia, Pa: Saunders, 2010.
Chadwick, Ruth, Darren Shickle, Henk Ten Have, and Urban Wiesing, eds. The Ethics of Genetic Screening. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-015-9323-6.
Bird, R. Curtis, and Bruce F. Smith, eds. Genetic Library Construction and Screening. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-642-56408-6.
F, Chadwick Ruth, ed. The ethics of genetic screening. Dordrecht: Kluwer Academic Publishers, 1999.
Juth, Niklas. Genetic information values and rights: The morality of presymptomatic genetic testing. Göteburg: Acta Universitatis Gothoburgensis, 2005.
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.
Sommer, Annemarie. Birth defects and genetic screening and counseling. Washington, D.C: Veterans Administration Central Office, Department of Medicine and Surgery, Agent Orange Projects Office, 1985.
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.
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.
1952-, Valverde Carlos, ed. Genetic screening of newborns: An ethical inquiry. Hauppauge, N.Y: Nova Science Publishers, 2009.
Workshop on Genetic Screening (1989 La Sapinière, Québec). Genetic screening: From newborns to DNA typing. Edited by Knoppers Bartha Maria, Laberge Claude M, Quebec Network of Genetic Medicine., New England Regional Screening Program., and Association Française de Prévention des Handicaps de l'Enfant. Amsterdam: Excerpta Medica, 1990.
Léon, Cassiers, and Vermeersch Etienne 1934-, eds. Erfelijkheid: Genetische tests en maatschappij. Leuven: Garant, 2000.
Gould, Randi L. Cancer and genetics: Answering your patients' questions. Huntington, NY: PRR, 1997.
Timmermans, Stefan. Saving babies?: The consequences of newborn genetic screening. Chicago: The University of Chicago Press, 2013.
1963-, Morrison Patrick J., Hodgson S. V, and Haites Neva E. 1947-, eds. Familial breast and ovarian cancer: Genetics, screening, and management. Cambridge, UK: Cambridge University Press, 2002.
1963-, Morrison Patrick J., Hodgson S. V, and Haites Neva E. 1947-, eds. Familial breast and ovarian cancer: Genetics, screening, and management. Cambridge: Cambridge University Press, 2005.
Ferris, Shauna. Genetic testing and insurance: International regulation. Sydney, Australia: School of Economic and Financial Studies, Macquarie University, 1997.
United States. Congress. Office of Technology Assessment., ed. Cystic fibrosis and DNA tests: Implications of carrier screening. Washington, DC: Congress of the U.S., Office of Technology Assessment, 1992.
Albany Birth Defects Symposium (16th 1985). Genetic disease: Screening and management: proceedings of the 1985 Albany Birth Defects Symposium, held in Albany, New York, September 30-October 1, 1985. Edited by Carter Thomas P. 1947- and Willey Ann M. New York: Liss, 1986.
Collins, Francis S. The language of life: DNA and the revolution in personalized medicine. New York: Harper, 2010.
Collins, Francis S. The language of life: DNA and the revolution in personalized medicine. New York: Harper, 2009.
Collins, Francis S. The Language of Life. New York: HarperCollins, 2010.
Jean-Louis, Reymond, ed. Enzyme assays: High-throughput screening, genetic selection, and fingerprinting. Weinheim, Germany: Wiley-VCH, 2006.
Ann, Baily Mary, and Murray Thomas H. 1946-, eds. Ethics and newborn genetic screening: New technologies, new challenges. Baltimore: Johns Hopkins University Press, 2009.
Ann, Baily Mary, and Murray Thomas H. 1946-, eds. Ethics and newborn genetic screening: New technologies, new challenges. Baltimore: Johns Hopkins University Press, 2009.
Royal College of Physicians of London., ed. Prenatal diagnosis and genetic screening: Community and service implications. London: Royal College of Physicians of London, 1989.
American Museum of Natural History. and Public Broadcasting Service (U.S.), eds. Our genes, our choices: Fred Friendly Seminars. [Alexandria, Va: PBS], 2003.
He, Jianzhi. Ji yin qi shi yu fa lü dui ce zhi yan jiu: A study of genetic discrimination and its legal responses. 8th ed. Beijing: Beijing da xue chu ban she, 2006.
United States. Congress. Office of Technology Assessment., ed. Genetic counseling and cystic fibrosis carrier screening: Results of a survey. Washington, DC: Congress of the U.S., Office of Technology Assessment, 1992.
Canada. Privacy Commissioner of Canada. Genetic testing and privacy. Ottawa, Ont: Privacy Commissioner of Canada, 1992.
National Academies Press (U.S.), National Cancer Policy Forum (U.S.), and National Cancer Policy Forum 2007., eds. Cancer-related genetic testing and counseling: Workshop proceedings. Washington, D.C: National Academies Press, 2007.
Kim, Ho-jung. array-CGH rŭl iyong han piso sepʻo pʻyeam ŭi chogi chaebal pʻyojija mit chindan mohyŏng kaebal =: Development of early-recurrence detection marker and diagnostic model using array-CGH in NSCLC. [Seoul]: Pogŏn Pokchibu, 2007.
Raz, Aviad E. Community genetics and genetic alliances: Eugenics, carrier testing, and networks of risk. Abingdon, Oxon: Routledge, 2009.
Michigan. Department of Community Health. Genetics through the life cycle: Improving health and preventing disease. 8th ed. Lansing, Mich: Michigan Dept. of Community Health, 2004.
New York State Task Force on Life and the Law. Genetic testing and screening in the age of genomic medicine. New York, N.Y: New York State Task Force on Life and the Law, 2000.
Dierickx, Kris. Genetisch gezond?: Ethische en sociale aspecten van genetische tests en screenings. Antwerpen: Intersentia, 1999.
Zakharov, I. A. GenEtika, ili, Rozhatʹ, nelʹzi︠a︡ klonirovatʹ. Novosibirsk: Izd-vo SO RAN, 2003.
Carlo, Bresciani, ed. Genetica e medicina predittiva: Verso un nuovo modello di medicina? Milano: Giuffrè, 2000.
Andrews, Lori B. Future perfect: Confronting decisions about genetics. New York: Columbia University Press, 2001.
Pearson, Virginia. Antenatal Genetic Screening. University of Bristol, Department of Social Medici, 1995.
Griffin, Darren K., and Gary L. Harton. Preimplantation Genetic Screening. Taylor & Francis Group, 2020.
Griffin, Darren K., and Gary L. Harton. Preimplantation Genetic Screening. Taylor & Francis Group, 2020.
Pupecki, Sandra R. Genetic Screening: New Research. Nova Science Publishers, 2006.
Pupecki, Sandra R. Focus on Genetic Screening Research. Nova Science Publishers, 2006.
Wiesing, Urban, Ruth F. Chadwick, Darren Shickle, and H. A. Ten Have. Ethics of Genetic Screening. Springer London, Limited, 2013.
Genetic screening and counselling. Philadelphia: Saunders, 2002.
Chadwick, Ruth, Urban Wiesing, Darren Shickle, and Henk Ten Have. The Ethics of Genetic Screening. Chadwick Ruth F Shickle Darren Ten Have H a, 2010.