Showing items related by title, author, creator and subject.

• Research on Familial Creutzfeldt--Jakob Disease (FCJD) Resulting in Presymptomatic Testing: Implications for the Human Genome Project 

  Ulm, Janet E.; Vnencak-Jones, Cindy L.; Bosque, Patrick (1993-03)
• GENETIC DISORDERS SOURCEBOOK: BASIC CONSUMER HEALTH INFORMATION ABOUT HEREDITARY DISORDERS, INCLUDING DISORDERS RESULTING FROM ABNORMALITIES IN SPECIFIC GENES, SUCH AS HEMOPHILIA, SICKLE CELL DISEASE, AND CYSTIC FIBROSIS, CHROMOSOMAL DISORDERS, SUCH AS DOWN SYNDROME, FRAGILE X SYNDROME, AND KLINEFELTER SYNDROME, AND COMPLEX DISORDERS WITH ENVIRONMENTAL AND GENETIC COMPONENTS, SUCH AS ALZHEIMER DISEASE, CANCER, HEART DISEASE, AND OBESITY, ALONG WITH INFORMATION ABOUT THE HUMAN GENOME PROJECT, GENETIC TESTING AND PRIVACY CONCERNS, THE SPECIAL NEEDS OF CHILDREN WITH GENETIC DISORDERS, CURRENT RESEARCH INITIATIVES, A GLOSSARY OF TERMS, AND A DIRECTORY OF RESOURCES FOR FURTHER HELP AND INFORMATION 

  Judd, Sandra J., ed. (2010)
• Notifying Patients Exposed to Blood Products Associated With Creutzfeldt-Jakob Disease: Integrating Science, Legal Duties and Ethical Mandates 

  Caulfield, Timothy; Dossetor, John; Boshkov, Lynn; Hannon, Judith; Sawyer, Douglas; Robertson, Gerald (1997-11-15)

  The issue of notifying people who have been exposed to blood products that have been associated with Creutzfeldt-Jakob disease (CJD) has arisen at a time when the Canadian blood system is under intense scrutiny. As a ...