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Paper Details

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.
Am J Hum Genet
145
2019
infant, pharmacogenomics variants, recessive, recessive diseases
Author NameAffiliation
Matthew S LeboBrigham and Women's Hospital, USA Harvard Medical School, USA The Broad Institute of MIT and Harvard
Timothy W YuHarvard Medical School, The Manton Center for Orphan Disease Research, Boston Children's Hospital
Timothy W YuHarvard Medical School, The Manton Center for Orphan Disease Research, Boston Children's Hospital
Casie A GenettiThe Manton Center for Orphan Disease Research, Boston Children's Hospital
Pankaj B AgrawalHarvard Medical School, The Manton Center for Orphan Disease Research, Boston Children's Hospital
Ingrid A HolmHarvard Medical School, The Manton Center for Orphan Disease Research, Boston Children's Hospital
Ingrid A HolmHarvard Medical School, The Manton Center for Orphan Disease Research, Boston Children's Hospital
Amy L McGuireCenter for Medical Ethics and Health Policy, Baylor College of Medicine
Robert C GreenHarvard Medical School, Brigham and Women's Hospital, USA The Broad Institute of MIT and Harvard
Heidi L RehmBrigham and Women's Hospital, USA Harvard Medical School, USA The Broad Institute of MIT and Harvard, USA Center for Genomic Medicine, Massachusetts General Hospital
Heidi L RehmBrigham and Women's Hospital, USA Harvard Medical School, USA The Broad Institute of MIT and Harvard, USA Center for Genomic Medicine, Massachusetts General Hospital
Alan H BeggsHarvard Medical School, The Manton Center for Orphan Disease Research, Boston Children's Hospital
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