Literature DB >> 10559037

The ethics and impact on behaviour of knowledge about one's own genome. Interview by Judy Jones.

M Levitt.   

Abstract

Mesh:

Year:  1999        PMID: 10559037      PMCID: PMC1129062          DOI: 10.1136/bmj.319.7220.1283

Source DB:  PubMed          Journal:  BMJ        ISSN: 0959-8138


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  10 in total

1.  Choosing who will be disabled: genetic intervention and the morality of inclusion.

Authors:  Allen Buchanan
Journal:  Soc Philos Policy       Date:  1996

2.  Ethical and cultural considerations in research on hereditary deafness.

Authors:  K M Grundfast; J Rosen
Journal:  Otolaryngol Clin North Am       Date:  1992-10       Impact factor: 3.346

Review 3.  Led (astray) by genetic maps: the cartography of the human genome and health care.

Authors:  A Lippman
Journal:  Soc Sci Med       Date:  1992-12       Impact factor: 4.634

Review 4.  Multiplex genetic testing. The Council on Ethical and Judicial Affairs, American Medical Association.

Authors: 
Journal:  Hastings Cent Rep       Date:  1998 Jul-Aug       Impact factor: 2.683

5.  Disclosure of Duchenne muscular dystrophy after newborn screening.

Authors:  E Parsons; D Bradley; A Clarke
Journal:  Arch Dis Child       Date:  1996-06       Impact factor: 3.791

6.  Psychosocial effects of screening for somatic risk: the Swedish alpha 1 antitrypsin experience.

Authors:  T F McNeil; T Sveger; T Thelin
Journal:  Thorax       Date:  1988-07       Impact factor: 9.139

7.  Uptake of cystic fibrosis testing in primary care: supply push or demand pull?

Authors:  H Bekker; M Modell; G Denniss; A Silver; C Mathew; M Bobrow; T Marteau
Journal:  BMJ       Date:  1993-06-12

8.  GIG response to the UK Clinical Genetics Society report "The genetic testing of children".

Authors:  S Dalby
Journal:  J Med Genet       Date:  1995-06       Impact factor: 6.318

9.  Genetic screening and ethics: European perspectives.

Authors:  R Chadwick; H ten Have; J Husted; M Levitt; T McGleenan; D Shickle; U Wiesing
Journal:  J Med Philos       Date:  1998-06

10.  Psychological consequences of neonatal screening for alpha 1-antitrypsin deficiency. Parental reactions to the first news of their infants' deficiency.

Authors:  T Thelin; T F McNeil; E Aspegren-Jansson; T Sveger
Journal:  Acta Paediatr Scand       Date:  1985-09
  10 in total
  1 in total

Review 1.  Genetic testing and insurance.

Authors:  A Murthy; A Dixon; E Mossialos
Journal:  J R Soc Med       Date:  2001-02       Impact factor: 5.344

  1 in total

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