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Nr. |
Eintrag |
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1 |
Colaianni, Alessandra; Chandrasekharan, Subhashini; Cook-Deegan, Robert Mullan:
Impact of patents and licensing practices on access to genetic testing and carrier screening for Tay-Sachs and Canavan disease
In: Gene patents and licensing practices and their impact on patient access to genetic tests / report of the Secretary's Advisory Committee on Genetics, Health, and Society. - Bethesda, Md. : Secretary's Advisory Committee on Genetics, Health, and Society, (2010). - H-1-H-18 |
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2 |
Valles, Sean A.:
The mystery of the mystery of common genetic diseases
In: Biology & Philosophy, 2010, Vol. 25 (2), 183-201 |
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3 |
Liou, Theodore G.; Rubenstein, Ronald C.:
Carrier screening, incidence of cystic fibrosis, and difficult decisions [editorial]
In: JAMA: The Journal of the American Medical Association, 2009, Vol. 302 (23), 2595-2596 |
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4 |
Delatycki, Martin B.:
Population screening for reproductive risk for single gene disorders in Australia: now and the future.
In: Twin Research and Human Genetics, 2008, Vol. 11 (4), 422-430 |
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5 |
Hegwer, G. et al.:
Knowledge and attitudes toward a free education and Ashkenazi Jewish carrier testing program
In: Journal of Genetic Counseling, 2006, Vol. 15 (1), 61-70 |
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6 |
Ross, Lainie Friedman:
Heterozygote carrier testing in high schools abroad: what are the lessons for the U.S.?
In: Journal of Law, Medicine and Ethics, 2006, Vol. 34 (4), 753-764 |
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7 |
Scriver, Charles R.; Mitchell, John J.:
Carrier screening of adolescents in Montreal
In: Living with the genome : ethical and social aspects of human genetics / ed. by Angus Clarke and Flo Ticehurst. - Houndmills [u.a.] : Palgrave Macmillan, (2006). - 122-129 |
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8 |
Bleich, J. David:
Genetic screening
In: Rosner, Fred, ed. Medicine and Jewish Law. Volume III. Brooklyn, NY: Yashar Books, Inc.; 2005: 55-82. |
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9 |
Fey, Toby Lee:
TECHNOLOGY AND TRADITION: JEWISH BIOETHICS IN THE AGE OF GENETICS
2001 |
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10 |
Bleich, J. David:
Genetic screening: survey of recent Halakhic periodical literature.
In: Tradition: A Journal of Orthodox Jewish Thought. , 2000, Vol. 34 (1), 63-87. |
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11 |
National Society of Genetic Counselors [NSGC] (United States):
Inherited diseases prevalent in Ashkenazi Jewish populations: understanding carrier screening options. A guide for education and decision making
In: In: Chicago, IL: National Society of Genetic Counselors, 1998, revised 2000 March: [19 p.]
2000 |
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12 |
Levin, Mark:
Screening Jews and Genes: A Consideration of the Ethics of Genetic Screening Within the Jewish Community: Challenges and Responses
In: Genetic Testing, 1999, Vol. 3 (2), 207-213 |
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13 |
Bowman, James E.:
To screen or not to screen: when should screening be offered?
In: Community Genetics. , 1998, Vol. 1 (3), 145-147. |
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14 |
Davis, Dena S.:
Discovery of Children's Carrier Status for Recessive Genetic Disease: Some Ethical Issues
In: Genetic Testing, 1998, Vol. 2 (4), 323-327 |
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15 |
Rhodes, Rosamond:
Genetic links, family ties, and social bonds: rights and responsibilities in the face of genetic knowledge.
In: Journal of Medicine and Philosophy. , 1998, Vol. 23 (1), 10-30. |
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16 |
Rothenberg, Karen H.; Rutkin, Amy B.:
Toward a framework of mutualism: the Jewish community in genetics research.
In: Community Genetics. , 1998, Vol. 1 (3), 148-153. |
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17 |
Dorff, Elliot N.:
Jewish theological and moral reflections on genetic screening: the case of BRCA1.
In: Health Matrix. , 1997, Vol. 7 (1), 65-96. |
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18 |
Edelson, Paul J.:
The Tay-Sachs disease screening program in the U.S. as a model for the control of genetic disease: an historical view.
In: Health Matrix. , 1997, Vol. 7 (1), 125-133. |
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19 |
Eng, Christine M. et al.:
Prenatal genetic carrier testing using triple disease screening.
In: JAMA. , 1997, Vol. 278 (15), 1268-1272. |
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20 |
Holtzman, Neil A.; Watson, Michael S.:
Promoting Safe and Effective Genetic Testing in the United States: Final Report of the Task Force on Genetic Testing.
In: In: Issued by the Task Force; 1997 Sep. 180 p.
1997 |
