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.