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

By Durkin M.E.   Keck-Waggoner C.L.   Popescu N.C.   Thorgeirsson S.S.  

Genomics, Vol. 73, Iss. 1, 2001-04 ,pp. : 20-27

Elsevier

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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

By Bayarsaihan D.   Dunai J.   Greally J.M.   Kawasaki K.   Sumiyama K.   Enkhmandakh B.   Shimizu N.   Ruddle F.H.  

Genomics, Vol. 79, Iss. 1, 2002-01 ,pp. : 137-143

Academic Press

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Genes for the CPE Receptor (CPETR1) and the Human Homolog of RVP1 (CPETR2) Are Localized within the Williams–Beuren Syndrome Deletion

By Paperna T.   Peoples R.   Wang Y-K.   Kaplan P.   Francke U.  

Genomics, Vol. 54, Iss. 3, 1998-12 ,pp. : 453-459

Academic Press

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Fine-Scale Comparative Mapping of the Human 7q11.23 Region and the Orthologous Region on Mouse Chromosome 5G: The Low-Copy Repeats That Flank the Williams-Beuren Syndrome Deletion Arose at Breakpoint Sites of an Evolutionary Inversion(s)

By Valero M.C.   de Luis O.   Cruces J.   Perez Jurado L.A.  

Genomics, Vol. 69, Iss. 1, 2000-10 ,pp. : 1-13

Elsevier

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Characterization and Expression Pattern of thefrizzledGeneFzd9,the Mouse Homolog ofFZD9Which Is Deleted in Williams-Beuren Syndrome

By Wang Y.-K.   Sporle R.   Paperna T.   Schughart K.   Francke U.  

Genomics, Vol. 57, Iss. 2, 1999-04 ,pp. : 235-248

Elsevier

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