Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes

Human Molecular Genetics

Volumn 7, Issue 12, 1998, Pages 1835-1840

  Wakamiya, Maki ^b   Lindsay, Elizabeth A ^a   Rivera Pérez, Jaime A ^b,c   Baldini, Antonio ^a   Behringer, Richard R ^b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF TEXAS   (United States)

^c CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN;

ANIMAL CELL; ARTICLE; BLADDER; BRAIN; CENTRAL NERVOUS SYSTEM; CONGENITAL HEART MALFORMATION; CRANIOFACIAL MALFORMATION; DIGEORGE SYNDROME; EMBRYO DEVELOPMENT; EYE; GENE; GENE DELETION; GENE EXPRESSION; GENE TARGETING; GENOME; HYPOPLASIA; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MOUSE; NONHUMAN; PARATHYROID GLAND; PATHOGENESIS; PONS; PRIMORDIAL GERM CELL; PRIORITY JOURNAL; PROTEIN EXPRESSION; STOMACH; TESTIS; THYMUS; THYROID GLAND; VELOCARDIOFACIAL SYNDROME;

ABNORMALITIES, MULTIPLE; ANIMALS; BRAIN; DIGEORGE SYNDROME; FEMALE; FERTILITY; GENE DELETION; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GOOSECOID PROTEIN; HOMEODOMAIN PROTEINS; IN SITU HYBRIDIZATION; MALE; MICE; MICE, INBRED C57BL; MICE, INBRED STRAINS; MICE, KNOCKOUT; MUTAGENESIS, SITE-DIRECTED; NUCLEAR PROTEINS; PREGNANCY; PROTEINS; REPRESSOR PROTEINS; RNA PROBES; SURVIVAL; SYNDROME; TRANSCRIPTION FACTORS;

EID: 0031767135     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.12.1835     Document Type: Article

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