Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Dissecting the genetics of common, complex disorders remains one of the great challenges in human genetics. The acceleration of human genome sequence determination, improvements in informatics, large-scale identification of single nucleotide polymorphisms and improvements in scoring technologies have now increased the feasibility of identifying polymorphisms that predispose to common disease.

Original publication

DOI

10.1016/s0959-437x(00)00075-7

Type

Journal article

Journal

Curr Opin Genet Dev

Publication Date

06/2000

Volume

10

Pages

330 - 334

Keywords

Chromosome Mapping, Genetic Diseases, Inborn, Genetics, Medical, Genome, Human, Humans, Polymorphism, Genetic