Novel identification of a four-base-pair deletion mutation in PITX2 in a Rieger syndrome family

Journal of Dental Research

Volumn 82, Issue 12, 2003, Pages 1008-1012

  Wang, Y ^a   Zhao, H ^b   Zhang, X ^a   Feng, H ^a  

^a PEKING UNIVERSITY SCHOOL AND HOSPITAL OF STOMATOLOGY   (China)

^b PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

Author keywords

Family; Gene mutation; Oligodontia; Rieger syndrome

Indexed keywords

HOMEODOMAIN PROTEIN; THREONINE; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR PITX2;

ADOLESCENT; ADULT; AGED; ARTICLE; BASE PAIRING; CHILD; CHINA; CRANIOFACIAL MALFORMATION; EXON; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENETICS; HUMAN; HYPODONTIA; MALE; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; STOP CODON; SYNDROME; TOOTH MALFORMATION;

ADOLESCENT; ADULT; AGED; ANODONTIA; BASE PAIRING; BASE SEQUENCE; CHILD; CHINA; CODON, TERMINATOR; CRANIOFACIAL ABNORMALITIES; EXONS; FEMALE; FRAMESHIFT MUTATION; HOMEODOMAIN PROTEINS; HUMANS; MALE; MUTATION; PEDIGREE; PHENOTYPE; SEQUENCE DELETION; SYNDROME; THREONINE; TOOTH ABNORMALITIES; TRANSCRIPTION FACTORS;

EID: 4344659834     PISSN: 00220345     EISSN: None     Source Type: Journal    
DOI: 10.1177/154405910308201214     Document Type: Article

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