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Paper Details

Genomic diagnosis for children with intellectual disability and/or developmental delay.
Genome Med
165
2017
Developmental disabilities, children, developmental delay, intellectual disability, neurological disease, pediatric neurological disease, whole-genome sequences
Author NameAffiliation
Kevin M BowlingHudsonAlpha Institute for Biotechnology
Susan M HiattHudsonAlpha Institute for Biotechnology
Kyle B BrothersUniversity of Louisville
Kelly M EastHudsonAlpha Institute for Biotechnology
Whitley V KelleyHudsonAlpha Institute for Biotechnology
Edward J LoseUniversity of Alabama at Birmingham
Carla A RichUniversity of Louisville
Shirley SimmonsUniversity of Alabama at Birmingham
Richard M MyersHudsonAlpha Institute for Biotechnology
Richard M MyersHudsonAlpha Institute for Biotechnology
Gregory S BarshHudsonAlpha Institute for Biotechnology
Elizabeth Martina BebinUniversity of Alabama at Birmingham
Gregory M CooperHudsonAlpha Institute for Biotechnology
Gregory M CooperHudsonAlpha Institute for Biotechnology
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink