Health insurance and the Genetic Information Nondiscrimination Act of 2008: Implications for public health policy and practice Read more about Health insurance and the Genetic Information Nondiscrimination Act of 2008: Implications for public health policy and practice
Reassessing insurers' access to genetic information: Genetic privacy, ignorance, and injustice Read more about Reassessing insurers' access to genetic information: Genetic privacy, ignorance, and injustice
Informed consent process in Alpha-1 testing of at-risk children: Views of parents and adults tested as children Read more about Informed consent process in Alpha-1 testing of at-risk children: Views of parents and adults tested as children
Social and ethical implications of BRCA testing Read more about Social and ethical implications of BRCA testing
Factors associated with experiences of genetic discrimination among individuals at risk for Huntington disease Read more about Factors associated with experiences of genetic discrimination among individuals at risk for Huntington disease
Regulatory and ethical issues on the utilization of FFPE tissues in research Read more about Regulatory and ethical issues on the utilization of FFPE tissues in research
Ordering genetic tests and interpreting the results Read more about Ordering genetic tests and interpreting the results
Genetic information: Acquisition, access, and control Read more about Genetic information: Acquisition, access, and control
Discrimination as a consequence of genetic testing Read more about Discrimination as a consequence of genetic testing
