Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
- Creator: 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.
- Resource Type: journal article
- Date: 2013
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
- Creator: Talseth-Palmer, B. A. , Bowden, N. A. , Scott, R. J. , Meldrum, C. , Nicholl, J. , Thompson, E. , Friend, K. , Liebelt, J. , Bratkovic, D. , Haan, E. , Yu, S.
- Resource Type: journal article
- Date: 2009