Integration of a c-myc Transgene Results in Disruption of the Mouse Gtf2ird1 Gene, the Homologue of the Human GTF2IRD1 Gene Hemizygously Deleted in Williams–Beuren Syndrome

Author:

Durkin Marian E.,Keck-Waggoner Catherine L.,Popescu Nicholas C.,Thorgeirsson Snorri S.

Publisher

Elsevier BV

Subject

Genetics

Reference31 articles.

1. Isolation and characterization of BEN, a member of the TFII-I family of DNA-binding proteins containing distinct helix-loop-helix domains;Bayarsaihan;Proc. Natl. Acad. Sci. USA,2000

2. Bridging cognition, the brain, and molecular genetics: Evidence from Williams syndrome;Bellugi;Trends Neurosci.,1999

3. Comparative mapping of the region of human chromosome 7 deleted in Williams syndrome;DeSilva;Genome Res.,1999

4. Williams–Beuren syndrome: Genes and mechanisms;Francke;Hum. Mol. Genet.,1999

5. Identification of GTF2IRD1, a putative transcription factor within the Williams–Beuren syndrome deletion at 7q11.23;Franke;Cytogenet. Cell Genet.,1999

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