A novel PITX2 mutation in non-syndromic orodental anomalies.
Oral Dis
; 24(4): 611-618, 2018 May.
Article
in En
| MEDLINE
| ID: mdl-29121437
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Tooth Abnormalities
/
Transcription Factors
/
Homeodomain Proteins
/
Mouth Abnormalities
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Female
/
Humans
/
Infant
/
Male
Language:
En
Journal:
Oral Dis
Journal subject:
ODONTOLOGIA
Year:
2018
Document type:
Article
Affiliation country:
Thailand
Country of publication:
Denmark