developmental defect during embryogenesis
rare syndrome with cardiac malformations
Monarch Disease Ontology release 2018-06-29
Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate
First reported adult patient with TARP syndrome: A case report
RBM10: Structure, functions, and associated diseases
TARP syndrome: Long-term survival, anatomic patterns of congenital heart defects, differential diagnosis and pathogenetic considerations