MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia

Journal of Dental Research

Volumn 82, Issue 12, 2003, Pages 1013-1017

  Nieminen, P ^a,d   Kotilainen, J ^a,c   Aalto, Y ^b   Knuutila, S ^b   Pirinen, S ^a,b   Thesleff, I ^d  

^a UNIVERSITY OF HELSINKI   (Finland)

^b HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^c Department of Health ^*  (Finland)

^d UNIVERSITY OF HELSINKI   (Finland)

Author keywords

Cleft palate; MSX1; Oligodontia; Tooth agenesis; Wolf Hirschhorn syndrome

Indexed keywords

HOMEODOMAIN PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR MSX1;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 4; CLEFT PALATE; CRANIOFACIAL MALFORMATION; FEMALE; FINLAND; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETICS; HAPLOIDY; HUMAN; HYPODONTIA; MALE; MULTIPLE MALFORMATION SYNDROME; MUTATION; PRESCHOOL CHILD; SYNDROME; TOOTH MALFORMATION;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; ANODONTIA; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 4; CLEFT PALATE; CRANIOFACIAL ABNORMALITIES; FEMALE; FINLAND; GENE DELETION; HAPLOIDY; HOMEODOMAIN PROTEINS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MSX1 TRANSCRIPTION FACTOR; MUTATION; SYNDROME; TOOTH ABNORMALITIES; TRANSCRIPTION FACTORS;

EID: 2342529911     PISSN: 00220345     EISSN: None     Source Type: Journal    
DOI: 10.1177/154405910308201215     Document Type: Article

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