Mice lacking the homologue of the human 22q11.2 gene CRLK phenocopy neurocristopathies of DiGeorge syndrome

Nature Genetics

Volumn 27, Issue 3, 2001, Pages 293-298

  Guris, Deborah L ^a   Fantes, Judith ^a   Tara, David ^b   Druker, Brian J ^b   Imamoto, Akira ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CELL MIGRATION; CHROMOSOME 22Q; CHROMOSOME MUTATION; DELETION MUTANT; DIGEORGE SYNDROME; EMBRYO; HETEROZYGOSITY; MOUSE; NEURAL CREST; NEURAL CREST CELL; NEURAL TUBE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; VELOCARDIOFACIAL SYNDROME;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ANIMALS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; DISEASE MODELS, ANIMAL; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HETEROZYGOTE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MICE; MICE, KNOCKOUT; NUCLEAR PROTEINS; PHENOTYPE; PHYSICAL CHROMOSOME MAPPING;

ANIMALIA;

EID: 0035098436     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/85855     Document Type: Article

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