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  1. Gene Mutation and Rescue in Congenital Diaphragmatic Hernia dbGaP

    ID: phs000485.v1.p1

    Description: Congenital Diaphragmatic Hernia (CDH) is a common and life-threatening malformation. The most common phenotype is left-sided posterolateral (Bochdalek...

  2. Patient-Specific Factors Influence Somatic Variations in VHL Tumors dbGaP

    ID: phs001107.v1.p1

    Description: Patients affected with von Hippel-Lindau disease are at risk of developing multiple independent clear cell renal carcinomas. This study performed whol...

    Study Types: Tumor vs. Matched-Normal

  3. Whole-Genome and Exome Sequencing in Clear-Cell Renal Cell Carcinoma dbGaP

    ID: phs000491.v1.p1

    Description: Study to evaluate the molecular genetics of ccRCC through integrative analyses of tumors and tumorgrafts using multiple platforms in clinically annota...

    Study Types: Case Set

  4. The Genomics and Randomized Trials Network (GARNET) Vitamin Intervention Stroke Prevention (VISP) trial dbGaP

    ID: phs000343.v1.p1

    Description: The VISP trial (PI Jim Toole, M.D., Wake Forest University School of Medicine) was a multi-center, double-blind, randomized, controlled clinical tria...

  5. NHLBI GO-ESP: Family Studies (Dilated Cardiomyopathy) dbGaP

    ID: phs000581.v1.p1

    Description: The NHLBI "Grand Opportunity" Exome Sequencing Project (GO-ESP), a signature project of the NHLBI Recovery Act investment, was designed to identify ge...

    Study Types: Case Set


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