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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

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A Single-Nucleotide Polymorphism of SMARCB1 in Human Breast Cancers

By Mimori K.   Inoue H.   Shiraishi T.   Ueo H.   Mafune K-i.   Tanaka Y.   Mori M.  

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Genes for the CPE Receptor (CPETR1) and the Human Homolog of RVP1 (CPETR2) Are Localized within the Williams–Beuren Syndrome Deletion

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PJA1, Encoding a RING-H2 Finger Ubiquitin Ligase, Is a Novel Human X Chromosome Gene Abundantly Expressed in Brain

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