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Nr. |
Eintrag |
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1 |
Mehlman, Maxwell J.:
Introduction to proceedings from a conference on newborn screening for nontreatable disorders.
In: Health Matrix, 2009, Vol. 19 (1), 137-139 |
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2 |
Simopoulos, Artemis P.:
Genetic screening: programs, principles, and research -- thirty years later. Reviewing the recommendations of the Committee for the Study of Inborn Errors of Metabolism (SIEM).
In: Public Health Genomics, 2009, Vol. 12 (2), 105-111 |
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3 |
Detmar, Symone et al.:
Parental opinions about the expansion of the neonatal screening programme
In: Community Genetics, 2008, Vol. 11 (1), 11-17 |
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4 |
Watthey, Lawrence W.; Boyd, Ann:
Genetic testing and moral freedom
In: Eubios Journal of Asian and International Bioethics, 2007, Vol. 17 (5), 142-144 |
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5 |
Ardaillou, R; Le Gall, JY:
Le dépistage néonatal généralisé par des tests d'analyse biologique
In: Bulletin de l'Académie nationale de médecine, 2006, Vol. 190 (8), 1745-1759 |
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6 |
Ardaillou, R; Le Gall, JY:
Le dépistage néonatal généralisé par des tests d'analyse biologique
2006 |
|
7 |
Mahowald, Mary Briody:
Preconception and prenatal decisions
In: In her: Bioethics and Women: Across the Life Span. Oxford; New York: Oxford University Press,, 2006, Vol. 2006, 73-91 |
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8 |
Pass, Kenneth A.:
Lessons learned from newborn screening for phenylketonuria
In: Genetics and public health in the 21st century : using genetic information to improve health and prevent disease / ed. by Muin J. Khoury ; Wylie Burke ; Elizabeth J. Thomson, 2000, 40, 385-404 |
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9 |
Paul, Diane B.:
PKU and procreative liberty : historical and ethical considerations
In: Ethical issues in health care on the frontiers of the twenty-first century / ed. by Stephen Wear ; James J. Bono ; Gerald Logue .., 2000, 65, 171-190 |
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10 |
Paul, Diane:
Contesting consent: the challenge to compulsory neonatal screening for PKU.
In: Perspectives in Biology and Medicine. , 1999, Vol. 42 (2), 207-219. |
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11 |
Paul, Diane B.:
PKU screening : competing agendas, converging stories
In: The practices of human genetics / ed. by Michael Fortun and Everett Mendelsohn, 1999, 21, 185-195 |
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12 |
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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13 |
Paul, Diane B.:
PKU screening : competing agendas, converging stories
In: The politics of heredity : essays on eugenics, biomedicine, and the nature-nurture debate / Diane B. Paul. - Albany, NY : State Univ. of New York Press, (1998). - 173-186 |
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14 |
Paul, Diane B.:
The Politics of Heredity: Essays on Eugenics, Biomedicine, and the Nature-Nurture Debate.
1998 |
|
15 |
Davis, Anne J. et al.:
Mental retardation.
In: > <their> Ethical Dilemmas and Nursing Practice. Fourth Edition. Stamford, CT: Appleton and Lange; 1997: 213-243. |
|
16 |
Génétique et temporalité
1997 |
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17 |
Motulsky, Arno G.:
Screening for genetic diseases. [Editorial].
In: New England Journal of Medicine. , 1997, Vol. 336 (18), 1314-1316. |
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18 |
Reilly, Philip R.:
Laws to regulate the use of genetic information.
In: > Rothstein, Mark A., ed. Genetic Secrets: Protecting Privacy and Confidentiality in the Genetic Era. New Haven, CT: Yale University Press; 1997: 369-391. |
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19 |
Geller, Lisa N. et al.:
Individual, family, and societal dimensions of genetic discrimination: a case study analysis.
In: Science and Engineering Ethics. , 1996, Vol. 2 (1), 71-88. |
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20 |
Hepburn, Elizabeth R.:
Genetic testing and early diagnosis and intervention: boon or burden?
In: Journal of Medical Ethics. , 1996, Vol. 22 (2), 105-110. |
