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Genetics

Ronald J A Trent
Med J Aust 2002; 176 (1): . || doi: 10.5694/j.1326-5377.2002.tb04251.x
Published online: 7 January 2002

One of the most significant medical developments in the past five years has been the completion of the Human Genome Project (HGP). The first draft of the human DNA sequence is now available. The discovery of new genes for a range of human genetic disorders, as well as genes for normal traits, will have far-reaching effects on diagnosis, treatment and prevention.1


  • University of Sydney at the Royal Prince Alfred Hospital, Sydney, NSW.


Correspondence: rtrent@med.usyd.edu.au

  • 1. Collins FS, McKusick VA. Implications of the Human Genome Project for medical science. JAMA 2001; 285: 540-544.
  • 2. DNA diagnosis of genetic disorders in Australasia — 10/06/00. <http://www.hgsa.com.au/> (follow link to DNA testing laboratories). Accessed September 2001.
  • 3. Pfost DR, Boyce-Jacino MT, Grant DM. A SNPshot: pharmacogenetics and the future of drug therapy. Trends Biotech 2000; 18: 3334-3338.
  • 4. Cavazzana-Calvo M, Hacein-Bey S, Yates F, et al. Gene therapy of human severe combined immunodeficiencies. J Gene Med 2001; 3: 201-206.
  • 5. Bell J. The new genetics and clinical practice. BMJ 1998; 316: 618-620.

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