So one child is waiting for adoption by Foster State Parents and again
Ancestry come forward with DNA to make a Family without "The Donner
Party"
Federal Register Volume 75, Number 216 (Tuesday, November 9, 2010)
On May 21, 2008, President George W. Bush signed the Genetic
Information Nondiscrimination Act of 2008 (``GINA''), Public Law 110-
233, 122 Stat. 881, codified at 42 U.S.C. 2000ff et seq., into law.
Congress enacted GINA in recognition of, among many achievements in the
field of genetics, the decoding of the human genome and the creation
and increased use of genomic medicine. As Congress noted, ``New
knowledge about genetics may allow for the development of better
therapies that are more effective against disease or have fewer side
effects than current treatments. These advances give rise to the
potential misuse of genetic information to discriminate in health
insurance and employment.'' GINA Section 2(1), 42 U.S.C. 2000ff, note.
Experts predict that the twenty-first century will see tremendous
strides in the new field of genomic medicine, bringing it into
mainstream medical practice. The National Human Genome Research
Institute (NHGRI), the institute within the National Institutes of
Health responsible for the mapping of the human genome, notes that ``by
identifying the genetic factors associated with disease, researchers
may be able to design more effective drugs; to prescribe the best
treatment for each patient; to identify and monitor individuals at high
risk from disease; and to avoid adverse drug reactions.'' NHGRI, The
Future of Genomic Medicine: Policy Implications for Research and
Medicine (Bethesda, Md. Nov. 16, 2005), available at
http://www.genome.gov/17516574 (last visited July 7, 2010).
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