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Page 1
Copy number variation in hereditary non-polyposis colorectal cancer.
Genes (Basel). 2013 Sep 26;4(4):536-55. doi: 10.3390/genes4040536.
Genes (Basel). 2013.
PMID: 24705261
Free PMC article.
Expanding the genetic basis of copy number variation in familial breast cancer.
Masson AL, Talseth-Palmer BA, Evans TJ, Grice DM, Hannan GN, Scott RJ.
Masson AL, et al.
Hered Cancer Clin Pract. 2014 May 24;12(1):15. doi: 10.1186/1897-4287-12-15. eCollection 2014.
Hered Cancer Clin Pract. 2014.
PMID: 24955146
Free PMC article.
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Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.
Talseth-Palmer BA, Holliday EG, Evans TJ, McEvoy M, Attia J, Grice DM, Masson AL, Meldrum C, Spigelman A, Scott RJ.
Talseth-Palmer BA, et al. Among authors: masson al.
BMC Med Genomics. 2013 Mar 26;6:10. doi: 10.1186/1755-8794-6-10.
BMC Med Genomics. 2013.
PMID: 23531357
Free PMC article.
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Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients.
Masson AL, Talseth-Palmer BA, Evans TJ, McElduff P, Spigelman AD, Hannan GN, Scott RJ.
Masson AL, et al.
Meta Gene. 2015 Dec 24;7:95-104. doi: 10.1016/j.mgene.2015.12.005. eCollection 2016 Feb.
Meta Gene. 2015.
PMID: 26909336
Free PMC article.
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