Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23

Cytogenetics and Cell Genetics

Volumn 86, Issue 3-4, 1999, Pages 296-304

  Franke, Y ^a   Peoples, R J ^a   Francke, Uta ^a,b,c  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^c STANFORD UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HELIX LOOP HELIX PROTEIN; TRANSCRIPTION FACTOR;

ALTERNATIVE RNA SPLICING; CHROMOSOME 7Q; CONFERENCE PAPER; GENE DELETION; HUMAN; MUSCLE; NORTHERN BLOTTING; OPEN READING FRAME; PHENOTYPE; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; SEQUENCE ANALYSIS; TRANSCRIPTION REGULATION; WILLIAMS BEUREN SYNDROME;

EID: 0032695657     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000015322     Document Type: Conference Paper

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