Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23

Cytogenetics and Cell Genetics

Volumn 82, Issue 3-4, 1998, Pages 238-246

  Peoples, R J ^a   Cisco, M J ^a   Kaplan, P ^b   Francke, U ^a,c  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c STANFORD UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; POLYGLUTAMIC ACID; TRANSCRIPTION FACTOR;

ALTERNATIVE RNA SPLICING; AMINO ACID SEQUENCE; ARTICLE; BINDING SITE; CASE REPORT; CHROMOSOME 7Q; CONTROLLED STUDY; DNA SEQUENCE; EXON; GENE DELETION; GENE EXPRESSION; GENE ISOLATION; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PRIORITY JOURNAL; PROTEIN DOMAIN; SEQUENCE HOMOLOGY; WILLIAMS BEUREN SYNDROME;

EID: 0032408489     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000015110     Document Type: Article

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