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A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.
Talseth-Palmer BA, Bowden NA, Meldrum C, Nicholl J, Thompson E, Friend K, Liebelt J, Bratkovic D, Haan E, Yu S, Scott RJ. Talseth-Palmer BA, et al. Among authors: bowden na. Cytogenet Genome Res. 2009;124(1):94-101. doi: 10.1159/000200093. Epub 2009 Apr 15. Cytogenet Genome Res. 2009. PMID: 19372674
Dysregulation of miRNA 181b in the temporal cortex in schizophrenia.
Beveridge NJ, Tooney PA, Carroll AP, Gardiner E, Bowden N, Scott RJ, Tran N, Dedova I, Cairns MJ. Beveridge NJ, et al. Hum Mol Genet. 2008 Apr 15;17(8):1156-68. doi: 10.1093/hmg/ddn005. Epub 2008 Jan 9. Hum Mol Genet. 2008. PMID: 18184693
Whole genome amplification and its impact on CGH array profiles.
Talseth-Palmer BA, Bowden NA, Hill A, Meldrum C, Scott RJ. Talseth-Palmer BA, et al. Among authors: bowden na. BMC Res Notes. 2008 Jul 29;1:56. doi: 10.1186/1756-0500-1-56. BMC Res Notes. 2008. PMID: 18710509 Free PMC article.
Gene expression profiling of xeroderma pigmentosum.
Bowden NA, Tooney PA, Scott RJ. Bowden NA, et al. Hered Cancer Clin Pract. 2006 May 15;4(2):103-10. doi: 10.1186/1897-4287-4-2-103. Hered Cancer Clin Pract. 2006. PMID: 20223010 Free PMC article.
69 results