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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Expression Analysis and Protein Localization of the Human HPC-1/Syntaxin 1A, a Gene Deleted in Williams Syndrome

By Botta A.   Sangiuolo F.   Calza L.   Giardino L.   Potenza S.   Novelli G.   Dallapiccola B.  

Genomics, Vol. 62, Iss. 3, 1999-12 ,pp. : 525-528

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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

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Identification of a Putative Transcription Factor Gene (WBSCR11) That Is Commonly Deleted in Williams-Beuren Syndrome

By Osborne L.R.   Campbell T.   Daradich A.   Scherer S.W.   Tsui L.-C.  

Genomics, Vol. 57, Iss. 2, 1999-04 ,pp. : 279-284

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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

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