Literature DB >> 15839036

Proposed international guidelines on ethical issues in medical genetics and genetic services (part I).

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Abstract

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Year:  1998        PMID： 15839036

Source DB:  PubMed          Journal:  Rev Derecho Genoma Hum        ISSN： 1134-7198


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  7 in total

Review 1.  Carrier screening for beta-thalassaemia: a review of international practice.

Authors:  Nicole E Cousens; Clara L Gaff; Sylvia A Metcalfe; Martin B Delatycki
Journal:  Eur J Hum Genet       Date:  2010-06-23       Impact factor: 4.246

2.  Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica.

Authors:  Karlene Mason; Felicea Gibson; Ruth-Ann Gardner; Beryl Serjeant; Graham R Serjeant
Journal:  J Community Genet       Date:  2015-12-02

3.  Genetic testing and private insurance--a case of "selling one's body"?

Authors:  D Hübner
Journal:  Med Health Care Philos       Date:  2006

4.  Public perspectives on informed consent for biobanking.

Authors:  Juli Murphy; Joan Scott; David Kaufman; Gail Geller; Lisa LeRoy; Kathy Hudson
Journal:  Am J Public Health       Date:  2009-10-15       Impact factor: 9.308

5.  Estimating and disclosing the risk of developing Alzheimer's disease: challenges, controversies and future directions.

Authors:  J Scott Roberts; Sarah M Tersegno
Journal:  Future Neurol       Date:  2010-07-01

6.  "He didn't say that thalassaemia might come up" - β-thalassaemia carriers' experiences and attitudes.

Authors:  Nicole E Cousens; Clara L Gaff; Sylvia A Metcalfe; Martin B Delatycki
Journal:  J Community Genet       Date:  2013-01-13

7.  Attitudes of physicians and patients towards disclosure of genetic information to spouse and first-degree relatives: a case study from Turkey.

Authors:  Aslihan Akpinar; Nermin Ersoy
Journal:  BMC Med Ethics       Date:  2014-05-16       Impact factor: 2.652
  7 in total

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