Stephanie Crofts

Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital Amaurosis

H. Hakonarson, Jun Wang, Yiran Guo, 2015, Ophthalmic genetics.

Juvenile idiopathic arthritis and uveitis in a paediatric Sydney population

Stephanie Crofts, K. Geering, 2012 .

Ocular and electrophysiological findings in a patient with Sly syndrome

J. Grigg, M. Flaherty, Stephanie Crofts, 2017, Ophthalmic genetics.

A negative waveform in the scotopic response in a patient with phosphoglycerate kinase deficiency: a visual electrophysiology report

Meredith Wilson, C. Troedson, J. Grigg, 2015, Documenta Ophthalmologica.

The development of aphakic glaucoma following lensectomy in congenital cataract in a NSW children's hospital

Stephanie Crofts, K. Geering, 2014 .

Spectrum of ocular disease in children aged between 0 and 3 years at an Australian paediatric tertiary hospital.

J. Grigg, R. Jamieson, Stephanie Crofts, 2023, Clinical & experimental ophthalmology.