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Results 1 - 10 of 13 for patient
  1. ... Initiative: New approaches for protecting research participants, particularly patients' privacy and the confidentiality of their data. Design ... of specialties, as well as people from the patient advocacy community, universities, pharmaceutical companies, and others. Opportunity ...
  2. ... a research study are usually not available to patients or their healthcare providers. Clinical testing, on the ... out about an inherited disorder in an individual patient or family. People receive the results of a ...
  3. ... by individual cells. Alternately, a sample of the patient's cells can be removed and exposed to ... containing the vector are then returned to the patient. If the treatment is successful, the new gene ...
  4. ... also needed databases to store large amounts of patient data efficiently. The Precision Medicine Initiative also raises ... or prevention approaches, and convey this knowledge to patients. Learn how to cite this page
  5. ... doctor or genetic counselor, or directly to the patient if requested. Newborn screening tests are done on ...
  6. ... interpret and explain. Therefore, it is important for patients and their families to ask questions about the ...
  7. ... DF, Turner NC. Circulating Tumor DNA Analysis in Patients With Cancer: American Society of Clinical Oncology and ...
  8. ... the Mediterranean Sea); or The name of a patient or family with the condition (for example, amyotrophic ...
  9. ... stressful and anxiety-producing. Health professional organizations and patient advocacy groups strongly recommend that people considering genetic ...
  10. ... these reasons, the National Institute on Aging and patient advocacy groups strongly recommend that people considering genetic ...
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