Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Raewyn Billings"'
Publikováno v:
Diagnostic Cytopathology.
Autor:
Katie A. Ashton, Nadine K. Berry, Ashleigh Fodeades, Raewyn Billings, Susan Dooley, Eva Chan, Cliff Meldrum, Kristen Palmer, Andrew Harland, Andrew Ziolkowski, Anoop K. Enjeti, Rodney J. Scott
Publikováno v:
Pathology. 54:S16-S17
Autor:
Beata Kozak-Klonowska, Tomasz Byrski, Jan Lubinski, Tomasz Huzarski, Andrzej Pławski, Magdalena Kuświk, Monika Siołek, E. Kilar, Katarzyna Golebiewska, Pawel Borun, Rodney J. Scott, Raewyn Billings, Helena Rudnicka, Dagmara Dymerska, Marek Szwiec, Grzegorz Kurzawski
Publikováno v:
Clinical Genetics. 92:649-653
It is well known that founder mutations associated with cancer risk have useful implications for molecular diagnostics. We report the presence of a founder mutation in EPCAM involved in the etiology of Lynch syndrome (LS). The mutation extends nearly
Autor:
Rodney J. Scott, Michael Hipwell, Katie A. Ashton, Raewyn Billings, Mary McPhillips, Katherine L. Tucker, Andrew Ziolkowski
Publikováno v:
Pathology. 53:S41
Autor:
Hossein Farahani, Adrian Wan, Raewyn Billings, Damian Yap, Samuel Aparicio, Anne-Marie Mes-Masson, Karey Shumansky, Daniel Lai, Camila P. E. de Souza, Sohrab P. Shah
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
Scientific Reports
Scientific Reports
Characterization and quantification of tumour clonal populations over time via longitudinal sampling are essential components in understanding and predicting the response to therapeutic interventions. Computational methods for inferring tumour clonal