Pallister-Hall syndrome phenotype in mice mutant for Gli3

Human Molecular Genetics

Volumn 11, Issue 9, 2002, Pages 1129-1135

  Böse, Jens ^a,b   Grotewold, Lars ^a   Rüther, Ulrich ^a  

^a HEINRICH HEINE UNIVERSITY   (Germany)

^b HELMHOLTZ CENTRE FOR INFECTION RESEARCH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR GLI3; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN;

ADRENAL DISEASE; ANIMAL CELL; ANIMAL MODEL; ANUS ATRESIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL FEATURE; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DISEASE MODEL; DNA BINDING; EMBRYO; EPIGLOTTIS; GASTROINTESTINAL DISEASE; GENE IDENTIFICATION; GENE MUTATION; GENE TARGETING; HOMOZYGOSITY; KIDNEY DISEASE; LARYNX DISORDER; MALFORMATION SYNDROME; MOUSE; NONHUMAN; ORGANOGENESIS; PALLISTER HALL SYNDROME; PATHOGENESIS; PHENOTYPE; POLYDACTYLY; PRIORITY JOURNAL; PROTEIN DOMAIN;

ANIMALIA;

EID: 0036566575     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/11.9.1129     Document Type: Article

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