| Authors: |
Arnett AB; Division of Developmental Medicine, Boston Children's Hospital, Brookline, MA; Department of Pediatrics, Harvard Medical School, Boston, MA; Department of Psychiatry, Harvard Medical School, Boston, MA. Electronic address: anne.arnett@childrens.harvard.edu., Koesterer R; The Broad Institute, Cambridge, MA., Tovar PG; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA., O'Connell M; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA., Patel S; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA., Zhang H; The Broad Institute, Cambridge, MA; Children's Rare Disease Collaborative, Boston Children's Hospital, Boston, MA., French CE; Children's Rare Disease Collaborative, Boston Children's Hospital, Boston, MA., Rockowitz S; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA; Children's Rare Disease Collaborative, Boston Children's Hospital, Boston, MA; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA., Flannick J; The Broad Institute, Cambridge, MA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA., Doan R; Department of Pediatrics, Harvard Medical School, Boston, MA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA. |
