Birth defects caused by mutations in human GLI3 and mouse Gli3 genes

Congenital Anomalies

Volumn 50, Issue 1, 2010, Pages 1-7

  Naruse, Ichiro ^a   Ueta, Etsuko ^a   Sumino, Yoshiki ^a   Ogawa, Masaya ^a   Ishikiriyama, Satoshi ^b  

^a TOTTORI UNIVERSITY   (Japan)

^b SHIZUOKA CHILDREN'S HOSPITAL   (Japan)

Author keywords

GCPS; Gli3; PAP A; Pdn; PHS; Xt

Indexed keywords

TRANSCRIPTION FACTOR GLI3;

AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; GENE MUTATION; GENE STRUCTURE; GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; HUMAN; NONHUMAN; PALLISTER HALL SYNDROME; PHENOTYPE; POLAND SYNDROME; POSTAXIAL POLYDACTYLY; PRIORITY JOURNAL; PROTEIN CLEAVAGE; REVIEW; SEQUENCE HOMOLOGY; ZINC FINGER MOTIF;

ABNORMALITIES, MULTIPLE; ANIMALS; CONGENITAL ABNORMALITIES; GENES, DOMINANT; GENES, RECESSIVE; HUMANS; KRUPPEL-LIKE TRANSCRIPTION FACTORS; MICE; MUTATION; NERVE TISSUE PROTEINS; PALLISTER-HALL SYNDROME; PHENOTYPE; POLYDACTYLY; SYNDACTYLY; ZINC FINGERS;

MUS;

EID: 77649226130     PISSN: 09143505     EISSN: 17414520     Source Type: Journal    
DOI: 10.1111/j.1741-4520.2009.00266.x     Document Type: Review

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