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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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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Identification of Genes from a 500-kb Region at 7q11.23 That Is Commonly Deleted in Williams Syndrome Patients

By Osborne L.R.   Martindale D.   Scherer S.W.   Shi X.M.   Huizenga J.   Heng H.H.Q.   Costa T.   Pober B.   Lew L.   Brinkman J.   Rommens J.   Koop B.   Tsui L.C.  

Genomics, Vol. 36, Iss. 2, 1996-09 ,pp. : 328-336

Academic Press

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A Novel Human Gene,WSTF,Is Deleted in Williams Syndrome

By Lu X.   Meng X.   Morris C.A.   Keating M.T.  

Genomics, Vol. 54, Iss. 2, 1998-12 ,pp. : 241-249

Elsevier

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A Mouse Single-Copy Gene,Gtf2i,the Homolog of HumanGTF2I,That Is Duplicated in the Williams-Beuren Syndrome Deletion Region

By Wang Y.-K.   Perez-Jurado L.A.   Francke U.  

Genomics, Vol. 48, Iss. 2, 1998-03 ,pp. : 163-170

Elsevier

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