Expanding the genetic basis of copy number variation in familial breast cancer

Por Masson, Amy L, Talseth-Palmer, Bente A, Evans, Tiffany-Jane, Grice, Desma M, Hannan, Garry N, Scott, Rodney J
Publicado em 2014

Copy Number Variation in Hereditary Non-Polyposis Colorectal Cancer

Por Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Grice, Desma M., Duesing, Konsta, Hannan, Garry N., Scott, Rodney J.
Publicado em 2013

Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients

Por Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, McElduff, Patrick, Spigelman, Allan D., Hannan, Garry N., Scott, Rodney J.
Publicado no Meta Gene (2015)

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

Por Talseth-Palmer, Bente A, Holliday, Elizabeth G, Evans, Tiffany-Jane, McEvoy, Mark, Attia, John, Grice, Desma M, Masson, Amy L, Meldrum, Cliff, Spigelman, Allan, Scott, Rodney J
Publicado em 2013