Important to test, important to support
Attitudes toward disability rights and prenatal diagnosis among leaders of support groups for genetic disorders in Israel
Datos Bibliográficos
| ID | 4589928 |
|---|---|
| Autores | A E Raz (0000-0001-6268-0409, Ben-Gurion University of the Negev, autor de correspondencia), Aviad Raz (0000-0001-9794-5470) |
| Año | 2004 |
| Volumen | 59 |
| Número | 9 |
| Páginas | 1857-1866 |
| Fecha de publicación | 2004-11-01 |
| Peer Reviewed | Sí |
| Open Access | Sí |
| Tipo | ARTICLE |
| Revista | Social Science & Medicine (JOURNAL) |
| Identificadores de la revista | ISSN: 0277-9536 • E-ISSN: 1873-5347 |
| Editorial | Elsevier BV (PUBLISHER) |
| DOI | 10.1016/j.socscimed.2004.02.016 |
| PMID | 15312920 |
| OpenAlex | W2042317148 |
| Idioma | EN |
| Citas recibidas | 36 |
| Referencias citadas | 31 |
Abortion · Context (archaeology · Geography · Human rights · Medical model of disability · Perspective (graphical · Political science · Pregnancy · Psychiatry · Sociology · Test (biology · Disability Rights and Representation · Ethics and Legal Issues in Pediatric Healthcare · Gender Studies · Law · Medicine · Prenatal Screening and Diagnostics · Psychology
The Rise of Genetic Couplehood? A Comparative View of Premarital Genetic Testing
Genetics, Disease, and Reproduction
On knowing and believing
‘The alien baby’
Children and Youth on the Front Line
Data Paradoxes
Imagined futures
Médecins israéliens face au diagnostic prénatal des fœtus intersexués
Genetic Responsibility in Germany and Israel
The Golden Helix
Divergent evolution of newborn screening
Coming to terms with the imperfectly normal child
Ashkenazi Jews
Lay perceptions of genetic testing in Germany and Israel
Disclosure of genetic information to relatives in Israel
Between social hypocrisy and social responsibility
Parents like me
Bereaved parents’ unwillingness to participate in a joint research interview
Balancing conceptions of disability in PND practices
Media and the Israeli disability rights legislation
Mapping the terrain of disability legislation
Genetically modified survival
Ethical implications for research into inclusive education in Arab societies
Without being in psychoanalysis I would never have dared to become pregnant”
Contextualizing geneticization and medical pluralism
Silenced voices
Views on disability and prenatal testing among families with Down syndrome and disability activists
Mothers' Continuing Bond With the Baby
Understandings of Down's syndrome
Uncertain prophecies
Carrier matching and collective socialization in community genetics
Bodies with New Organs
Genetic Counseling for Sex Chromosome Anomalies (SCAs) in Israel and Germany
Decision-Making and Ante-Natal Screening for Sickle Cell and Thalassaemia Disorders
Eugenic utopias/dystopias, reprogenetics, and community genetics
The Geneticization of Autism
Love’s Labor
Power and Powerlessness in Jewish History
Abortion Approval as a Ritual of Symbolic Control
Special Supplement
Prenatal Testing and Disability Rights
The Future of the Disabled in Liberal Society
Reproducing Jews
Whose right to choose? The 'new' genetics, prenatal testing and people with learning difficulties
The Perils of Compensation in Social Welfare Policy
Who Causes the Blind to See
Ethical Aspects of Genetic Screening in Israel
From Lineage to Sexual Mores
Eugenics Is Alive and Well
Enabling Disability
| Obras citantes distintas | 36 |
|---|---|
| Citas por año | 1,64 |
| Intervalo de citas | 2004 - 2023 (20) |
| Velocidad de citación | historical |
| Altamente citado | No |
| Tipos de cita | Neutras: 35 |