Libri sul tema "Genetic screening"
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Fischer, Michael W., e Markus Hengstschläger. Genetic screening. Frankfurt am Main: Peter Lang, 2009.
Bioethics, Nuffield Council on, a cura di. Genetic screening: Ethical issues. London: Nuffield Council on Bioethics, 1993.
Gregg, Anthony R., e Joe Leigh Simpson. Genetic screening and counseling. Philadelphia: W.B. Saunders Co., 2002.
Gregg, Anthony R., e Joe Leigh Simpson. Genetic screening and counseling. Philadelphia, Pa: Saunders, 2010.
Chadwick, Ruth, Darren Shickle, Henk Ten Have e Urban Wiesing, a cura di. The Ethics of Genetic Screening. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-015-9323-6.
Bird, R. Curtis, e Bruce F. Smith, a cura di. 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, a cura di. 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., a cura di. Genetic monitoring and screening in the workplace. Washington, DC: Congress of the U.S., Office of Technology Assessment, 1990.
1952-, Valverde Carlos, a cura di. 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. A cura di Knoppers Bartha Maria, Laberge Claude M, Quebec Network of Genetic Medicine., New England Regional Screening Program. e Association Française de Prévention des Handicaps de l'Enfant. Amsterdam: Excerpta Medica, 1990.
Léon, Cassiers, e Vermeersch Etienne 1934-, a cura di. 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 e Haites Neva E. 1947-, a cura di. Familial breast and ovarian cancer: Genetics, screening, and management. Cambridge, UK: Cambridge University Press, 2002.
1963-, Morrison Patrick J., Hodgson S. V e Haites Neva E. 1947-, a cura di. 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., a cura di. 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. A cura di Carter Thomas P. 1947- e 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, a cura di. Enzyme assays: High-throughput screening, genetic selection, and fingerprinting. Weinheim, Germany: Wiley-VCH, 2006.
Ann, Baily Mary, e Murray Thomas H. 1946-, a cura di. Ethics and newborn genetic screening: New technologies, new challenges. Baltimore: Johns Hopkins University Press, 2009.
Ann, Baily Mary, e Murray Thomas H. 1946-, a cura di. Ethics and newborn genetic screening: New technologies, new challenges. Baltimore: Johns Hopkins University Press, 2009.
Royal College of Physicians of London., a cura di. Prenatal diagnosis and genetic screening: Community and service implications. London: Royal College of Physicians of London, 1989.
American Museum of Natural History. e Public Broadcasting Service (U.S.), a cura di. 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. 8a ed. Beijing: Beijing da xue chu ban she, 2006.
United States. Congress. Office of Technology Assessment., a cura di. 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.) e National Cancer Policy Forum 2007., a cura di. 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. 8a 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, a cura di. 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., e Gary L. Harton. Preimplantation Genetic Screening. Taylor & Francis Group, 2020.
Griffin, Darren K., e 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 e 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 e Henk Ten Have. The Ethics of Genetic Screening. Chadwick Ruth F Shickle Darren Ten Have H a, 2010.