YANG, N, MACARTHUR, DG, WOLDE, B, ONYWERA, VO, BOIT, MK, LAU, SYM-A, WILSON, RH, SCOTT, RA, PITSILADIS, YP, NORTH, K. The ACTN3 R577X Polymorphism in East and West African Athletes.
Medicine & Science in Sports & Exercise
Jones, KJ, North, KN. External ophthalmoplegia in neuromuscular disorders: Case report and review of the literature.
Lek, A, Evesson, FJ, Sutton, RB, North, KN, Cooper, ST. Ferlins: Regulators of Vesicle Fusion for Auditory Neurotransmission, Receptor Trafficking and Membrane Repair.
O'Grady, GL, Ma, A, Sival, D, Wong, MTY, Peduto, T, Menezes, MP, Young, H, Waddell, L, Ghaoui, R, Needham, M, et al. Prominent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related disease.
European Journal of Human Genetics
Oates, EC, Payne, JM, Foster, SL, Clarke, NF, North, KN. Young Australian adults with NF1 have poor access to health care, high complication rates, and limited disease knowledge.
American Journal of Medical Genetics Part A