Paper Chase is a research database designed to offer abstracts of research articles published in journals that have a highly rated impact factor as determined by ISI Impact Factor and PageRank. Abstracts are organized by date, with the most recently published papers listed first. 

Paper Chase

Copy number variation and human genome maps.

Nat. Genet.. 4 30, 2010;42(5):365-6.
McCarroll SA.

Department of Genetics, Harvard Medical School, Boston, Massachusetts, USA. mccarroll@genetics.med.harvard.edu

Abstract:

Maps of human genome copy number variation (CNV) are maturing into useful resources for complex disease genetics. Four new studies increase the resolution of CNV maps and seek to locate human phenotypic variation on these maps.