 |
|
Ophthalmic GeneticsAt the Dawn of Discovery
Leslie Hyman, PhD;
Barbara Klein, MD, MPH;
Barbara Nemesure, PhD;
Janey Wiggs, MD, PhD
Arch Ophthalmol. 2007;125(1):9-10.
|
|
| Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. |
|
|
|
Now this is not the end. It is not even the beginning of the end. But it is, perhaps, the end of the beginning.—Winston Churchill, 1942
Ophthalmic genetics is undergoing a major transformation. The role of heredity in ocular disease has been explored for more than 100 years, with the early focus on conditions that could be identified specifically as straightforward mendelian inherited disorders. In these disorders replication of the trait is easily observed, and clear-cut probabilities of transmission can be readily calculated. The discovery of DNA and advances in DNA-related technologies have led to significant advances in the genetics of all diseases (and traits), including those affecting the visual system. Progress in the field has accelerated, aided by the completion of the Human Genome Project in 2003 and the International HapMap Project in 2005. . . . [Full Text of this Article]
AUTHOR INFORMATION
 CiteULike  Connotea  Del.icio.us  Digg  Reddit  Technorati  Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
|
Microsatellite analysis of the GLC1B locus on chromosome 2 points to NCK2 as a new candidate gene for normal tension glaucoma
Akiyama et al.
Br J Ophthalmol 2008;92:1293-1296.
ABSTRACT
| FULL TEXT
|
