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Prologue Genetics and Genomic Health Care: The Mission and Aims of the National Human Genome Research Institute and Its Potential Impact on Clinical Practices | p. vii |
Introduction Genetics and Ethics in Nursing: New Questions in the Age of Genomic Health | p. xiii |
Coda Genetics and Genomics in Historical Context A Brief History of the Early Days of Clinical Genetics | p. xix |
How Far We Have Come | p. xx |
Genetics, Genomics, and Ethics: Basic Considerations | p. 1 |
The ANA Code of Ethics | p. 5 |
Integrating Ethical Guidelines with Scope and Standards of Genetics and Genomics Nursing Practice | p. 13 |
Shaping Genetic Policy: The United States Initiatives | p. 27 |
Principles of Healthcare Ethics for the Twenty-first Century | p. 53 |
Redefining the Conventions of Informed Consent: Challenges in the Genomic Era | p. 65 |
Genetic Inheritance, Identity, and the Proper Role of Nursing | p. 79 |
Danger and Genomic Technologies | p. 97 |
Religious and Cultural Perspectives of Communities and Societies | p. 103 |
Hinduism and Sikhism: Genetic Counseling Aspects | p. 109 |
"Every Generation...": A Jewish Approach to Questions of Genetic Research, Testing and Screening, and Gene Therapy | p. 129 |
The Catholic Church Views on Genetic Testing: Indications for Genetic Counselors | p. 141 |
Attitudes of Muslims Regarding the New Genetics: Testing, Treatment, and Technology | p. 149 |
Genetics and Ethics from a Christian Perspective | p. 165 |
Native American Communities: Perspectives on Healthcare Genetics | p. 179 |
Hispanic/Latino Perspectives on Genetics and Ethics | p. 201 |
African American Perspectives on Genetics and Ethics | p. 213 |
Applications of Genetics and Genomics in Health Care | p. 235 |
Concerns of Patients and Families Surrounding Genetic Testing | p. 241 |
Parental Request for Advanced Directives: Decision-Making in Evolving Environments | p. 251 |
Ethical Analysis of Genetic Testing in Children | p. 265 |
Genetics and Ethics in Nursing: Cancer Prevention for Clients with Inherited Cancer Risk | p. 285 |
Ethical Obligations to Patients Who Engage in Lifelong Self-surveillance for Genetic Risk of Cancer | p. 301 |
Cystic Fibrosis: Screening, Testing, Ethics | p. 315 |
Genetic Testing and Counseling in Huntington Disease | p. 331 |
Case Studies in Genetics and Ethics | p. 345 |
Prenatal Case Study | p. 349 |
Sickle Cell Disease Case Study | p. 359 |
Case Study in Hereditary Breast and Ovarian Cancer | p. 369 |
Hereditary Nonpolyposis Colon Cancer: A Case Study of Ethical Implications | p. 385 |
The P Family, At Risk for Alzheimer's Disease | p. 397 |
Epilogue Genetics and Ethics in Health Care and Nursing | p. 407 |
Glossary of Terms | p. 417 |
Acronyms | p. 423 |
Contributor Biographies | p. 429 |
Index | p. 443 |
Table of Contents provided by Ingram. All Rights Reserved. |
The New copy of this book will include any supplemental materials advertised. Please check the title of the book to determine if it should include any access cards, study guides, lab manuals, CDs, etc.
The Used, Rental and eBook copies of this book are not guaranteed to include any supplemental materials. Typically, only the book itself is included. This is true even if the title states it includes any access cards, study guides, lab manuals, CDs, etc.