-
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
-
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
-
Ramchand, J, Wallis, M, Farouque, O, Trainer, A, Macciocca, I, Lynch, E, Martyn, M, Phelan, D, Chong, B, Zentner, D, et al.
A Prospective Evaluation of Whole-Exome Sequencing in Idiopathic Dilated Cardiomyopathy and Related Phenotypes.
Heart Lung and Circulation
27:
s48
2018
view publication
-
Metcalfe, SA, Martyn, M, Ames, A, Anderson, V, Archibald, AD, Couns, GDG, Carter, R, Cohen, J, Cotter, M, GenCouns, M, et al.
Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screening.
Genetics in Medicine
19(12)
:
1346 -1355
2017
view publication
-
Downie, L, Halliday, JL, Burt, RA, Lunke, S, Lynch, E, Martyn, M, Poulakis, Z, Gaff, C, Sung, V, Wake, M, et al.
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort.
BMJ Paediatrics Open
1(1)
:
e000119
2017
view publication