Isolation of a putative transcriptional regulator from the region of 22q11 deleted in digeorge syndrome, shprintzen syndrome and familial congenital heart disease

Human Molecular Genetics

Volumn 2, Issue 12, 1993, Pages 2099-2107

  Halford, Stephanle ^a   Wadey, Roy ^a   Roberts, Catherine ^a   Daw, Sara C M ^a   Whiting, Jennifer A ^a   O'donnell, Hllary ^a   Dunham, Ian ^a,b   Bentley, David ^a,b   Lindsay, Elizabeth ^a,c   Baldini, Antonio ^a,c   Francis, Fiona ^a,d   Lehrach, Hans ^a,d   Williamson, Robert ^a,e   Wilson, David I ^a,f   Goodship, Judith ^a,f   Cross, Ian ^a,f   Burn, John ^a,f   Scambler, Peter J ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b KING'S COLLEGE LONDON   (United Kingdom)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

^e IMPERIAL COLLEGE LONDON   (United Kingdom)

^f NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MURINAE;

GENE PRODUCT; PROTEIN;

ARTICLE; CHROMOSOME 22Q; CONGENITAL HEART DISEASE; DIGEORGE SYNDROME; EMBRYO DEVELOPMENT; GENE DELETION; GENE EXPRESSION; HUMAN; HUMAN CELL; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; TRANSCRIPTION REGULATION; VELOCARDIOFACIAL SYNDROME; YEAST;

ABNORMALITIES, MULTIPLE; AMINO ACID SEQUENCE; ANIMAL; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; COMPARATIVE STUDY; CONSENSUS SEQUENCE; DIGEORGE SYNDROME; EMBRYO AND FETAL DEVELOPMENT; ENHANCER ELEMENTS (GENETICS); GENOMIC LIBRARY; HEART DEFECTS, CONGENITAL; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; MICE; MOLECULAR SEQUENCE DATA; MULTIGENE FAMILY; POLYMERASE CHAIN REACTION; SEQUENCE DELETION; SEQUENCE HOMOLOGY, AMINO ACID; SUPPORT, NON-U.S. GOV'T; TRANSCRIPTION FACTORS; TRANSDUCIN; TRANSLOCATION (GENETICS);

EID: 0027731681     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/2.12.2099     Document Type: Article

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