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Paper Details

Children's rare disease cohorts: an integrative research and clinical genomics initiative.
NPJ Genom Med
39
2020
Children, GLS, epilepsy, exomes, genomes, genomically, inflammatory bowel disease, patient, pediatric rare disease, rare disease
Author NameAffiliation
Ingrid A HolmThe Manton Center for Orphan Disease Research, Boston Children's Hospital
Ingrid A HolmBoston Children's Hospital
Ingrid A HolmHarvard Medical School
Ingrid A HolmThe Manton Center for Orphan Disease Research, Boston Children's Hospital
Ingrid A HolmHarvard Medical School
Ingrid A HolmBoston Children's Hospital
Catherine A BrownsteinThe Manton Center for Orphan Disease Research, Boston Children's Hospital
Catherine A BrownsteinBoston Children's Hospital
Catherine A BrownsteinHarvard Medical School
Catherine A BrownsteinThe Manton Center for Orphan Disease Research, Boston Children's Hospital
Catherine A BrownsteinHarvard Medical School
Catherine A BrownsteinBoston Children's Hospital
Susan KornetskyBoston Children's Hospital
Alan H BeggsThe Manton Center for Orphan Disease Research, Boston Children's Hospital
Alan H BeggsHarvard Medical School
Alan H BeggsBoston Children's Hospital
Timothy W YuThe Manton Center for Orphan Disease Research, Boston Children's Hospital
Timothy W YuBoston Children's Hospital
Timothy W YuHarvard Medical School
Timothy W YuThe Manton Center for Orphan Disease Research, Boston Children's Hospital
Timothy W YuHarvard Medical School
Timothy W YuBoston Children's Hospital
Piotr SlizBoston Children's Hospital
Piotr SlizThe Manton Center for Orphan Disease Research, Boston Children's Hospital
Piotr SlizHarvard Medical School
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