The MurineCYLN2Gene: Genomic Organization, Chromosome Localization, and Comparison to the Human Gene That Is Located within the 7q11.23 Williams Syndrome Critical Region

By Hoogenraad C.C.   Eussen B.H.J.   Langeveld A.   van Haperen R.   Winterberg S.   Wouters C.H.   Grosveld F.   De Zeeuw C.I.   Galjart N.  

Genomics, Vol. 53, Iss. 3, 1998-11 ,pp. : 348-358

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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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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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

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A Physical Map of the Mouseshaker-2Region Contains Many of the Genes Commonly Deleted in Smith-Magenis Syndrome (del17p11.2p11.2)

By Probst F.J.   Chen K.-S.   Zhao Q.   Wang A.   Friedman T.B.   Lupski J.R.   Camper S.A.  

Genomics, Vol. 55, Iss. 3, 1999-02 ,pp. : 348-352

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