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

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

Elsevier

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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)

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

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Human EMR2, a Novel EGF-TM7 Molecule on Chromosome 19p13.1, Is Closely Related to CD97

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Localization of Chl1-Related Helicase Genes to Human Chromosome Regions 12p11 and 12p13: Similarity between Parts of These Genes and Conserved Human Telomeric-Associated DNA

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