STUDY: Next Generation Mendelian Genetics: Kabuki Syndrome

Study Description

The ultimate purpose of this research is to identify genes causing hereditary disorders. We are scaling a new approach to identify the... Show More

Study Accession Alternative Stable ID type
phs000295.v1.p1 dbGaP Exome Sequencing

Who controls access to this study

National Human Genome Research Institute
Access information: http://grants.nih.gov/grants/gwas

Publications

20711175

Data provider(s)

  • Title Name Institute
    Principal Investigators Deborah Nickerson, PhD Department of Genome Sciences, University of Washington, Seattle, WA, USA
    Principal Investigators Jay Shendure, PhD Department of Genome Sciences, University of Washington, Seattle, WA, USA
    Principal Investigators Michael Bamshad, MD Department of Pediatrics, University of Washington, Seattle, WA, USA
    Funding Source 1RC2 HG005608-01 National Institutes of Health, Bethesda, MD, USA
    Funding Source 1R01HD048895 National Institutes of Health, Bethesda, MD, USA

Who archives the data?

The database of Genotypes and Phenotypes (dbGaP)