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Copy number variation in hereditary non-polyposis colorectal cancer.
Masson AL, Talseth-Palmer BA, Evans TJ, Grice DM, Duesing K, Hannan GN, Scott RJ. Masson AL, et al. Among authors: scott rj. Genes (Basel). 2013 Sep 26;4(4):536-55. doi: 10.3390/genes4040536. Genes (Basel). 2013. PMID: 24705261 Free PMC article.
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: scott rj. BMC Res Notes. 2008 Jul 29;1:56. doi: 10.1186/1756-0500-1-56. BMC Res Notes. 2008. PMID: 18710509 Free PMC article.
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: scott rj. Cytogenet Genome Res. 2009;124(1):94-101. doi: 10.1159/000200093. Epub 2009 Apr 15. Cytogenet Genome Res. 2009. PMID: 19372674
A multicenter blinded study to evaluate KRAS mutation testing methodologies in the clinical setting.
Whitehall V, Tran K, Umapathy A, Grieu F, Hewitt C, Evans TJ, Ismail T, Li WQ, Collins P, Ravetto P, Leggett B, Salto-Tellez M, Soong R, Fox S, Scott RJ, Dobrovic A, Iacopetta B. Whitehall V, et al. Among authors: scott rj. J Mol Diagn. 2009 Nov;11(6):543-52. doi: 10.2353/jmoldx.2009.090057. Epub 2009 Oct 8. J Mol Diagn. 2009. PMID: 19815694 Free PMC article.
731 results