Uwechue IC - Search Results

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An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome.

Blair HJ, Uwechue IC, Barsh GS, Rowe PS, Boyd Y. Blair HJ, et al. Among authors: uwechue ic. Genomics. 1998 Feb 15;48(1):128-31. doi: 10.1006/geno.1997.5144. Genomics. 1998. PMID: 9503026

A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1.

Reed V, Rider S, Maslen GL, Hatchwell E, Blair HJ, Uwechue IC, Craig IW, Laval SH, Monaco AP, Boyd Y. Reed V, et al. Among authors: uwechue ic. Genomics. 1994 Apr;20(3):341-6. doi: 10.1006/geno.1994.1186. Genomics. 1994. PMID: 8034305

The mouse X-linked developmental mutant, tattered, lies between DXMit55 and Xkh and is associated with hyperkeratinization.

Uwechue IC, Cooper BF, Goble C, Hacker T, Blair HJ, Burke DT, Herman G, Boyd Y. Uwechue IC, et al. Genomics. 1996 Oct 15;37(2):238-41. doi: 10.1006/geno.1996.0549. Genomics. 1996. PMID: 8921395

Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis.

Blair HJ, Gormally E, Uwechue IC, Boyd Y. Blair HJ, et al. Among authors: uwechue ic. Hum Mol Genet. 1998 Mar;7(3):549-55. doi: 10.1093/hmg/7.3.549. Hum Mol Genet. 1998. PMID: 9467016

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