Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene.

Journal of medical genetics

Volumn 41, Issue 2, 2004, Pages

  Ghassibe M ^a   Revencu, N ^a   Bayet, B ^a   Gillerot, Y ^a   Vanwijck, R ^a   Verellen Dumoulin, C ^a   Vikkula, M ^a  

^a DE DUVE INSTITUTE   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; DNA BINDING PROTEIN; INTERFERON REGULATORY FACTOR; IRF6 PROTEIN, HUMAN; PROTEIN; TRANSCRIPTION FACTOR;

ARTICLE; CHROMOSOME 1; CLEFT LIP; CLEFT PALATE; CONGENITAL MALFORMATION; DOMINANT GENE; FEMALE; FOOT MALFORMATION; GENETIC LINKAGE; GENETICS; HUMAN; HYPODONTIA; LIP; MALE; METABOLISM; MULTIPLE MALFORMATION SYNDROME; MUTATION; PALATE; PEDIGREE; PROTEIN BINDING; PROTEIN TERTIARY STRUCTURE; SYNDROME;

ABNORMALITIES, MULTIPLE; ANODONTIA; CHROMOSOMES, HUMAN, PAIR 1; CLEFT LIP; CLEFT PALATE; DNA; DNA-BINDING PROTEINS; FEMALE; FOOT DEFORMITIES, CONGENITAL; GENES, DOMINANT; HUMANS; INTERFERON REGULATORY FACTORS; LINKAGE (GENETICS); LIP; MALE; MUTATION; PEDIGREE; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; PROTEINS; SYNDROME; TRANSCRIPTION FACTORS; UVULA;

MLCS; MLOWN;

EID: 17644442804     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2003.009274     Document Type: Article

References (0)