Książki na temat „Genetic screening”

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

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

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

Chadwick, Ruth, Darren Shickle, Henk Ten Have i Urban Wiesing, red. The Ethics of Genetic Screening. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-015-9323-6.

Bird, R. Curtis, i Bruce F. Smith, red. 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, red. 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, i Vermeersch Etienne 1934-, red. Erfelijkheid: Genetische tests en maatschappij. Leuven: Garant, 2000.

United States. Congress. Office of Technology Assessment., red. 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, red. 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, i Simpson Joe Leigh 1943-, red. 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. Redaktorzy Knoppers Bartha Maria, Laberge Claude M, Quebec Network of Genetic Medicine., New England Regional Screening Program. i Association Française de Prévention des Handicaps de l'Enfant. Amsterdam: Excerpta Medica, 1990.

1952-, Valverde Carlos, red. 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, red. 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., red. Screening for Down's syndrome. Cambridge: Cambridge University Press, 1994.

American Museum of Natural History. i Public Broadcasting Service (U.S.), red. 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.) i National Cancer Policy Forum 2007., red. Cancer-related genetic testing and counseling: Workshop proceedings. Washington, D.C: National Academies Press, 2007.

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

Royal College of Physicians of London., red. Prenatal diagnosis and genetic screening: Community and service implications. London: Royal College of Physicians of London, 1989.

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

Jean-Louis, Reymond, red. 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. Wyd. 8. 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, red. Genetica e medicina predittiva: Verso un nuovo modello di medicina? Milano: Giuffrè, 2000.

United States. Congress. Office of Technology Assessment., red. 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., i Willey Ann M, red. 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, i Thompson Janna 1942-, red. The sorting society: The ethics of genetic screening and therapy. Cambridge: Cambridge University Press, 2008.

Daniela, Freitag, Karner Sandra i Universität für Bildungswissenschaften Klagenfurt. Interuniversitäres Forschungsinstitut für Fernstudien der Österreichischen Universitäten. Arbeitsbereich Technik- und Wissenschaftsforschung, red. 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., i Gary L. Harton. Preimplantation Genetic Screening. Taylor & Francis Group, 2020.

Griffin, Darren K., i 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 i 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 i 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.