TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly

Cleft Palate-Craniofacial Journal

Volumn 49, Issue 2, 2012, Pages 240-244

  Kaewkhampa, Arunee ^a   Jotikasthira, Dhirawat ^a   Malaivijitnond, Sutti ^b   Kantaputra, Piranit ^a  

^a CHIANG MAI UNIVERSITY   (Thailand)

^b Nan Hospital   (Thailand)

Author keywords

Ankyloglossia; Carpal bone anomaly; Cleft lip and palate; Hypodontia; Hypoplastic thumb; Limb anomalies; TBX22; Tongue tie; Tooth agenesis

Indexed keywords

NUCLEIC ACID BINDING PROTEIN; T BOX PROTEIN 22; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ANKYLOGLOSSIA; ARTICLE; CASE REPORT; CHILD; CLEFT LIP PALATE; CONTROLLED STUDY; DISEASE ASSOCIATION; EXON; GENE STRUCTURE; GENETIC ASSOCIATION; HUMAN; HYPODONTIA; LIMB MALFORMATION; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; PHENOTYPIC VARIATION; PREMOLAR TOOTH; PRIORITY JOURNAL; SCHOOL CHILD; CLEFT LIP; CLEFT PALATE; GENETICS; HAND MALFORMATION; MOUTH DISEASE; PHENOTYPE;

ANODONTIA; CHILD; CLEFT LIP; CLEFT PALATE; HAND DEFORMITIES, CONGENITAL; HUMANS; MALE; MOUTH ABNORMALITIES; MUTATION, MISSENSE; PHENOTYPE;

EID: 84858612750     PISSN: 10556656     EISSN: 15451569     Source Type: Journal    
DOI: 10.1597/10-208     Document Type: Article

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