-
Kondrashova, O, Au-Yeung, G, Leas, L, Ho, G-Y, Lunke, S, Alsop, K, Scott, C, Hamilton, A, Ananda, S, Freimund, A, et al.
Abstract B35: Australian Ovarian Cancer Assortment Trial–Allocating ovarian cancer patients into clinical trials based on molecular profiling.
Clinical Cancer Research
24(15_Supplement)
:
b35 -b35
2018
view publication
-
Woodcock, IR, Menezes, MP, Coleman, L, Yaplito-Lee, J, Peters, H, White, SM, Stapleton, R, Phelan, DG, Chong, B, Lunke, S, et al.
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome..
Semin Pediatr Neurol
26:
2 -9
2018
view publication
-
Sung, V, Downie, L, Halliday, J, Burt, R, Lunke, S, Lynch, E, Martyn, M, Poulakis, Z, Gaff, C, Wake, M, et al.
Whole exome sequencing in infants with congenital hearing loss..
2018
view publication
-
Dillon, OJ, Lunke, S, Stark, Z, Yeung, A, Thorne, N, Melbourne Genomics Health Alliance, Gaff, C, White, SM, Tan, TY.
Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders..
Eur J Hum Genet
26(5)
:
644 -651
2018
view publication
-
Stark, Z, Lunke, S, Brett, GR, Tan, NB, Stapleton, R, Kumble, S, Yeung, A, Phelan, DG, Chong, B, Fernandez, MF, et al.
Rapid genomic testing in acute paediatric care: Is it worth the trouble?.
Pathology
50:
s59
2018
view publication