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Murtha, Michael T

TitleYearPMID
De novo mutations revealed by whole-exome sequencing are strongly associated with autism. 2012 22495306
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. 2011 21658581
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 2008 18587394
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