Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects

Human Molecular Genetics

Volumn 10, Issue 22, 2001, Pages 2549-2556

  Funke, Birgit ^a   Epstein, Jonathan A ^b   Kochilas, Lazaros K ^b   Lu, Min Min ^b   Pandita, Raj K ^a   Liao, Jun ^a   Bauerndistel, Ralf ^c   Schüler, Tanja ^c   Schorle, Hubert ^c   Brown, M Christian ^d   Adams, Joe ^d   Morrow, Bernice E ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c KARLSRUHE INSTITUTE OF TECHNOLOGY   (Germany)

^d HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOPROTEIN IB;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; CARDIOVASCULAR MALFORMATION; CELL VIABILITY; CHROMOSOME 22Q; CHROMOSOME DELETION; CHRONIC OTITIS MEDIA; CIRCLING BEHAVIOR; CLINICAL FEATURE; CONGENITAL DISORDER; DIGEORGE SYNDROME; DISEASE ASSOCIATION; DYSPLASIA; EAR MALFORMATION; GENE FUNCTION; GENE OVEREXPRESSION; HAPLOIDY; HEMIZYGOSITY; HUMAN; HUMAN CELL; HYPOPLASIA; INNER EAR; MIDDLE EAR; NONHUMAN; PERCEPTION DEAFNESS; PRIORITY JOURNAL; THYMUS; TRANSGENE; TRANSGENIC MOUSE;

ANIMALIA; BACTERIA (MICROORGANISMS); MUS MUSCULUS;

EID: 0035888654     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.22.2549     Document Type: Article

References (37)

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