Libros sobre el tema "Genetic screening"

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

Gregg, Anthony R., and Joe Leigh Simpson. Genetic screening and counseling. Philadelphia, Pa: Saunders, 2010.

Bioethics, Nuffield Council on, ed. Genetic screening: Ethical issues. London: Nuffield Council on Bioethics, 1993.

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, Dept. of Medicine and Surgery, Agent Orange Projects Office, 1985.

Léon, Cassiers, and Vermeersch Etienne 1934-, eds. Erfelijkheid: Genetische tests en maatschappij. Leuven: Garant, 2000.

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.

United States. Veterans Administration. Agent Orange Projects Office, ed. Birth defects and genetic screening and counseling. Washington, D.C: Veterans Administration Central Office, Department of Medicine and Surgery, Agent Orange Projects Office, 1985.

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

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.

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

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

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

Ferris, Shauna. Genetic testing and insurance: International regulation. Sydney, Australia: School of Economic and Financial Studies, Macquarie University, 1997.

Collins, Francis S. The Language of Life. New York: HarperCollins, 2010.

Collins, Francis S. The language of life: DNA and the revolution in personalized medicine. New York: Harper, 2010.

G, Grudzinskas J., ed. Screening for Down's syndrome. Cambridge: Cambridge University Press, 1994.

American Museum of Natural History. and Public Broadcasting Service (U.S.), eds. Our genes, our choices: Fred Friendly Seminars. [Alexandria, Va: PBS], 2003.

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.

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.

Ann, Baily Mary, and Murray Thomas H. 1946-, eds. Ethics and newborn genetic screening: New technologies, new challenges. Baltimore: Johns Hopkins University Press, 2009.

Jean-Louis, Reymond, ed. Enzyme assays: High-throughput screening, genetic selection, and fingerprinting. Weinheim, Germany: Wiley-VCH, 2006.

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.

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.

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.

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.

1947-, Carter Thomas P., and Willey Ann M, eds. Genetic disease: Screening and management: proceedings of the 1985 Albany Birth Defects Symposium, held in Albany, New York, September 30-October 1, 1985. New York: Liss, 1986.

Gutkind, Lee. An immense new power to heal: The promise of personalized medicine. Pittsburgh, PA: In Fact Books, 2012.

Loane, Skene, and Thompson Janna 1942-, eds. The sorting society: The ethics of genetic screening and therapy. Cambridge: Cambridge University Press, 2008.

Daniela, Freitag, Karner Sandra, and Universität für Bildungswissenschaften Klagenfurt. Interuniversitäres Forschungsinstitut für Fernstudien der Österreichischen Universitäten. Arbeitsbereich Technik- und Wissenschaftsforschung, eds. Diffusion und Organisation genetischen Testens: Medizinische ExpertInnen im Interview. Klagenfurt: IFF-Arbeitsbereich "Technik- und Wissenschaftsforschung", 2007.

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.

Danieli, Gian Antonio. Genetics and genomics for the cardiologist. Dordrecht: Kluwer Academic Pub., 2002.

Pupecki, Sandra R. Genetic Screening: New Research. Nova Science Publishers, 2006.

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.

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.

Genetic screening and counseling. Philadelphia: W.B. Saunders Co., 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.

Genomic tests for ovarian cancer detection and management. Rockville, MD: U.S. Department of Health and Human Services, Public Health Service, Agency for Healthcare Research and Quality, 2006.