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Franke, Y; Peoples, R J; Francke, U (1999) Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23. Cytogenet Cell Genet 86:296-304
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Ring, H Z; Vameghi-Meyers, V; Nikolic, J M et al. (1999) Mapping of the KHSRP gene to a region of conserved synteny on human chromosome 19p13.3 and mouse chromosome 17. Genomics 56:350-2
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Ring, H Z; Vameghi-Meyers, V; Min, H et al. (1999) The mouse Fubp gene maps near the distal end of chromosome 3. Genomics 56:357-8
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Ring, H Z; Chang, H; Guilbot, A et al. (1999) The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5q. Hum Genet 104:326-32
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Ring, H Z; Vameghi-Meyers, V; Wang, W et al. (1998) Five SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin (SMARC) genes are dispersed in the human genome. Genomics 51:140-3
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Paperna, T; Peoples, R; Wang, Y K et al. (1998) Genes for the CPE receptor (CPETR1) and the human homolog of RVP1 (CPETR2) are localized within the Williams-Beuren syndrome deletion. Genomics 54:453-9
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Wang, Y K; Perez-Jurado, L A; Francke, U (1998) A mouse single-copy gene, Gtf2i, the homolog of human GTF2I, that is duplicated in the Williams-Beuren syndrome deletion region. Genomics 48:163-70
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Peoples, R J; Cisco, M J; Kaplan, P et al. (1998) Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23. Cytogenet Cell Genet 82:238-46
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Gebe, J A; Kiener, P A; Ring, H Z et al. (1997) Molecular cloning, mapping to human chromosome 1 q21-q23, and cell binding characteristics of Spalpha, a new member of the scavenger receptor cysteine-rich (SRCR) family of proteins. J Biol Chem 272:6151-8
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Liu, W; Faraco, J; Qian, C et al. (1997) The gene for microfibril-associated protein-1 (MFAP1) is located several megabases centromeric to FBN1 and is not mutated in Marfan syndrome. Hum Genet 99:578-84
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