Article
A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®).
Human mutation - 1 May 2011
Amberger Joanna, Bocchini Carol, Hamosh Ada
Abstract excerpt
OMIM's task of cataloging the association between human phenotypes and their causative genes (the Morbid Map of the Genome) and classifying and naming newly recognized disorders is growing rapidly. Establishing the relationship between genotype and phenotype has become increasingly complex. New technologies such as genome-wide association studies (GWAS) and array comparative genomic hybridization (aCGH) define...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.