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Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project
Authors:Ozge Ceyhan-Birsoy  Jaclyn B. Murry  Kalotina Machini  Matthew S. Lebo  Timothy W. Yu  Shawn Fayer  Casie A. Genetti  Talia S. Schwartz  Pankaj B. Agrawal  Richard B. Parad  Ingrid A. Holm  Amy L. McGuire  Robert C. Green  Heidi L. Rehm  Alan H. Beggs
Affiliation:1. Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA;2. Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Cambridge, MA 02139, USA;3. Department of Pathology, Brigham and Women’s Hospital, Boston, MA 02115, USA;4. Harvard Medical School, Boston, MA 02115, USA;5. Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children’s Hospital, Boston, MA 02115, USA;6. Department of Neurology, Boston Children’s Hospital, Boston, MA 02115, USA;7. Division of Genetics, Department of Medicine, Brigham and Women’s Hospital, Boston, MA 02115, USA;8. Division of Newborn Medicine, Boston Children’s Hospital, Boston, MA 02115, USA;9. Department of Pediatric Newborn Medicine, Brigham and Women’s Hospital, Boston, MA 02115, USA;10. Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, TX 77030, USA;11. The Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA;12. Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA
Abstract:
Keywords:whole-exome sequencing  genomic sequencing  newborn  newborn screening  newborn sequencing
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