Type

Journal Article

A survey of medical directors of life insurance companies concerning use of genetic information

View online source

Authors:

McEwen, Jean E.

McCarty, Katharine

Reilly, Philip R.

Year:

1993

Am J Hum Genet

Return to Search Results

Share

Related Publications

Book

Enabling biotechnological inventions in Europe and the United States: A study of the patentability of proteins and DNA sequences with special emphasis on the disclosure requirement
Book

Disclosure dilemmas: Ethics of genetic prognosis after the 'right to know/not to know' debate
Book Chapter

The social consequences of genetic disclosure
Book Chapter

Disclosure of familial risk in genetic testing
Book Chapter

Confidentiality, disclosure, and recontact
Book Chapter

Information disclosure and consent
Book Chapter

Without disclosure, no informed choice
Journal Article

Genetic fallout: New technologies are changing the legal landscape
Journal Article

Disclosure of genetic information within families
Journal Article

Offering individual genetic research results: Context matters
Journal Article

Genetic counselor opinions of, and experiences with telephone communication of BRCA1/2 test results
Journal Article

Your biobank, your doctor? The right to full disclosure of population biobank findings
Journal Article

Time for DNA disclosure
Journal Article

Clinical obligations and public health programmes: Healthcare provider reasoning about managing the incidental results of newborn screening
Journal Article

Confronting the stigma of eugenics: Genetics, demography and the problems of population
Journal Article

Handling ethical, legal and social issues in birth cohort studies involving genetic research: Responses from studies in six countries
Journal Article

BRCA1/2 test results impact risk management attitudes, intentions, and uptake
Journal Article

Ethical considerations in first-trimester Down syndrome risk assessment
Journal Article

Comparison of participant information and informed consent forms of five European studies in genetic isolated populations
Journal Article

What is a meaningful result? Disclosing the results of genomic research in autism to research participants
Journal Article

Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing
Journal Article

On the development of a decision support intervention for mothers undergoing BRCA1/2 cancer genetic testing regarding communicating test results to their children
Journal Article

The disclosure of genetic information: A human research ethics perspective
Journal Article

Researcher perspectives on disclosure of incidental findings in genetic research
Journal Article

Returning individual research results: Development of a cancer genetics education and risk communication protocol
Journal Article

Educational advantage
Journal Article

Understanding preferences for disclosure of individual biomarker results among participants in a longitudinal birth cohort
Journal Article

Disclosure of the genetic risk of Alzheimer's disease
Journal Article

Time for full and frank data disclosure
Journal Article

Did I really want to know this? Pregnant women's reaction to detection of a soft marker during ultrasound screening

+