Condition: Abnormality of the dentition


rs768663992 in CLUAP1 gene and Abnormality of the dentition PMID 28679688 2017 Compound heterozygous alterations in intraflagellar transport protein CLUAP1 in a child with a novel Joubert and oral-facial-digital overlap syndrome.

rs139455627 in TSPEAR gene and Abnormality of the dentition PMID 27736875 2016 Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.

rs1569151872 in TSPEAR-AS1;TSPEAR gene and Abnormality of the dentition PMID 27736875 2016 Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.