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Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing
- Singh, Ashish Kumar, Talseth-Palmer, Bente, Xavier, Alexandre, Scott, Rodney J., Drabløs, Finn, Sjursen, Wenche
- Vogelezang, Suzanne, Bradfield, Jonathan P., Early Growth Genetics Consortium,, Grant, Sturan F. A., Felix, Janine F., Jaddoe, Vincent W. V., Pennell, Craig E., Wang, Carol
Erythrocyte microRNA sequencing reveals differential expression in relapsing-remitting multiple sclerosis
- Groen, Kira, Maltby, Vicki E., Lea, Rodney A., Sanders, Katherine A., Fink, J. Lynn, Scott, Rodney J., Tajouri, Lotti, Lechner-Scott, Jeannette
Basal-like breast cancer: molecular profiles, clinical features and survival outcomes
- Milioli, Heloisa H., Tishchenko, Inna, Riveros, Carlos, Berretta, Regina, Moscato, Pablo
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
- 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.
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