A database of genetic variants of uncertain significance (VUS) which may be pathogenic in Lynch Syndrome patients http://t.co/cSZhXBSDs2
Just published, "The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome", LOVD-powered. A nice... http://t.co/LUScxktgGW
RT @JohnMHancock: The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome http://t.co/6svsEGzd9Y
The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome http://t.co/6svsEGzd9Y
RT @DrKhouryCDC: Lynch Syndrome repository of gene variant and disease information http://t.co/1NHvUYPhs1
RT @LizSzabo: RT @DrKhouryCDC: Lynch Syndrome repository of gene variant & disease information http://t.co/Yv80k5m7zq @brian_mansfield
RT @DrKhouryCDC: Lynch Syndrome repository of gene variant & disease information http://t.co/Yv80k5m7zq @brian_mansfield
Lynch Syndrome repository of gene variant and disease information http://t.co/1NHvUYPhs1
I'm reading The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome http://t.co/cSZhXBSDs2 #springerlink