GENETICS IN MEDICAL PRACTIC
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Аннотация:
Medical genetics has been formally recognized as a medical specialty in the United States only within the past decade. Initially, medical genetics was concerned with relatively rare single gene or chromosomal disorders, but with the sequencing of the human genome, genetics has become the driving force in medical research and is now poised for integration into medical practice. This article offers a perspective on the role of genetics in medical practice and how this role may evolve over the next several years. The author classifies the genetic contribution to medical practice into three categories: monogenic or chromosomal disorders, more common disorders due to a monogenic or single gene mutation, and common multifactorial disorders in which the interaction of multiple genes and the environment contribute to the cause of the condition.
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F.S. Collins Shattuck lecture: medical and societal consequences of the Human Genome Project 1:STN:280:DyaK1M3psVelug%3D%3D 10.1056/NEJM199907013410106 N Engl J Med, 341 (1999), pp. 28-37 Google Scholar
N.A. Holtzman, T.M. Marteau Will genetics revolutionize medicine? B. Childs, D. Valle Genetics, biology and disease 1:CAS:528:DC%2BD3cXnsVaku78%3D 10.1146/annurev.genom.1.1.1 Annu Rev Genomics Hum Genet, 1 (2000), pp. 1-19 Google Scholar
J.G. Hall, E.K. Powers, R.T. Mcllvaine, V.H. Ean The frequency and financial burden of genetic disease in a pediatric hospital 1:STN:280:DyaE1c3gvVCnug%3D%3D 10.1002/ajmg.1320010405 Am J Med Genet, 1 (1978), pp. 417-436 Google Scholar
S.J. Hayflick, M.P. Eiff, L. Carpenter, J. Steinberger Primary care physicians' utilization and perceptions of genetics services 1:STN:280:DC%2BD3M7lvF2jtQ%3D%3D 10.1097/00125817-199811000-00005 Genet Med, 1 (1998), pp. 13-21 Google Scholar