Condition: Pierre Robin Syndrome
rs1057519389
in
EBF3
gene and
Pierre Robin Syndrome
PMID 28017370
2017 De Novo Mutations in EBF3 Cause a Neurodevelopmental Syndrome.
PMID 28017372
2017 A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3.