Identification of a Van Der Woude Syndrome mutation in the Cleft Palate 1 mutant mouse

Genesis

Volumn 48, Issue 5, 2010, Pages 303-308

  Stottmann, R W ^a   Bjork, B C ^a   Doyle, J B ^a   Beier, David R ^a  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

Cleft palate; Craniofacial development; ENU mutagenesis; Irf6; Mouse

Indexed keywords

INTERFERON REGULATORY FACTOR 6;

ACETYLATOR PHENOTYPE; AMINO ACID SUBSTITUTION; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CLEFT PALATE 1 GENE; CONTROLLED STUDY; EMBRYO; GENE; GENETIC SCREENING; MISSENSE MUTATION; MOLECULAR CLONING; MOUSE; MOUSE MUTANT; MUTATIONAL ANALYSIS; NONHUMAN; PHENOTYPIC VARIATION; POINT MUTATION; PRIORITY JOURNAL; SKELETON MALFORMATION; TONGUE; VAN DER WOUDE SYNDROME; WILD TYPE;

ALLELES; AMINO ACID SEQUENCE; ANIMALS; CLEFT PALATE; DISEASE MODELS, ANIMAL; DNA MUTATIONAL ANALYSIS; EMBRYO, MAMMALIAN; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENETIC PREDISPOSITION TO DISEASE; HINDLIMB; HUMANS; INTERFERON REGULATORY FACTORS; MICE; MICE, INBRED STRAINS; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY, AMINO ACID; SYNDROME;

EID: 77952056955     PISSN: 1526954X     EISSN: 1526968X     Source Type: Journal    
DOI: 10.1002/dvg.20618     Document Type: Article

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