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

Access to resources Recommend Favorite

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

Elsevier

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Elsevier

Access to resources Recommend Favorite