STUDY: Genetic Analysis of Limb Malformation Disorders: Miller Syndrome Sequencing Study (LMD-MS)

Study Description

The overall goal of this project is to investigate the etiology and pathogenesis of malformations (i.e., birth defects) of the limb,... Show More

Study Accession Alternative Stable ID type
phs000244.v1.p1 dbGaP Exome Sequencing; Pedigree Whole Genome Sequencing

Who controls access to this study

National Heart, Lung, and Blood Institute DAC
Access information: http://grants.nih.gov/grants/gwas

Publications

501501
7452413
20220176
19915526
19892942

Data provider(s)

  • Title Name Institute
    Principal Investigators Michael Bamshad, MD Seattle Children's, Seattle, WA, USA
    Principal Investigators Leroy Hood, MD, PhD Institute for Systems Biology, Seattle, WA, USA
    Principal Investigators David Galas, PhD Institute for Systems Biology, Seattle, WA, USA
    Funding Source Institute for Systems Biology Program University of Luxembourg, Luxembourg
    Funding Source 5R01HL094976 National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, USA

Who archives the data?

The database of Genotypes and Phenotypes (dbGaP)