A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®).

Abstract

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… (More)
DOI: 10.1002/humu.21466

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