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Genetic variation and its role in malignancy.
Talseth-Palmer BA, Scott RJ. Talseth-Palmer BA, et al. Among authors: scott rj. Int J Biomed Sci. 2011 Sep;7(3):158-71. Int J Biomed Sci. 2011. PMID: 23675233 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
Combined analysis of three Lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers.
Talseth-Palmer BA, Wijnen JT, Brenne IS, Jagmohan-Changur S, Barker D, Ashton KA, Tops CM, Evans TJ, McPhillips M, Groombridge C, Suchy J, Kurzawski G; Dutch Cancer Genetics Group; Spigelman A, Møller P, Morreau HM, Van Wezel T, Lubinski J, Vasen HF, Scott RJ. Talseth-Palmer BA, et al. Among authors: scott rj. Int J Cancer. 2013 Apr 1;132(7):1556-64. doi: 10.1002/ijc.27843. Epub 2012 Oct 11. Int J Cancer. 2013. PMID: 22987364 Free article.
731 results