Genomic Organization of the Genes Gtf2ird1, Gtf2i, and Ncf1 at the Mouse Chromosome 5 Region Syntenic to the Human Chromosome 7q11.23 Williams Syndrome Critical Region-Reference-Cited by-同舟云学术

Genomic Organization of the Genes Gtf2ird1, Gtf2i, and Ncf1 at the Mouse Chromosome 5 Region Syntenic to the Human Chromosome 7q11.23 Williams Syndrome Critical Region

Published:2002-01 Issue:1 Volume:79 Page:137-143
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Bayarsaihan Dashzeveg,Dunai Judit,Greally John M.,Kawasaki Kazuhiko,Sumiyama Kenta,Enkhmandakh Badam,Shimizu Nobuyoshi,Ruddle Frank H.

Publisher

Elsevier BV

Subject

Genetics

Reference37 articles.

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3. Identification of a novel slow-muscle-fiber enhancer binding protein, MusTRD1;O'Mahoney;Mol. Cell. Biol.,1998

4. Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome;Osborne;Genomics,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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