Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Frontiers in Ophthalmology|July 10, 2024
The Prevalence of Glaucoma in the Jirel Ethnic Group of NepalSarah Miller, Nicholas B Blackburn, Matthew Johnson, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 12, 2017
Common genetic variation within miR-146a predicts disease onset and relapse in multiple sclerosisYuan Zhou, Ming Chen, Steve Simpson, et al.
Human Genetics|September 17, 2008
Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel lociKathryn P Burdon, Douglas J Coster, Jac C Charlesworth, et al.
American Journal of Obstetrics and Gynecology|December 11, 2007
Genetic association of preeclampsia to the inflammatory response gene SEPS1Eric K Moses, Matthew P Johnson, Linda Tømmerdal, et al.
Oncology Reports|October 30, 2014
A retrospective examination of mean relative telomere length in the Tasmanian Familial Hematological Malignancies StudyNicholas B Blackburn, Jac C Charlesworth, James R Marthick, et al.
Investigative Ophthalmology & Visual Science|September 28, 2005
Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigreeJac C Charlesworth, Thomas D Dyer, Jim M Stankovich, et al.
Investigative Ophthalmology & Visual Science|May 8, 2009
Heritability of central corneal thickness in nuclear familiesJohn A Landers, Alex W Hewitt, David P Dimasi, et al.
Scientific Reports|July 18, 2023
The association between disability progression, relapses, and treatment in early relapse onset MS: an observational, multi-centre, longitudinal cohort studyValery Fuh-Ngwa, Jac C Charlesworth, Yuan Zhou, et al.
Scientific Reports|December 21, 2017
Impact of the G84E variant on HOXB13 gene and protein expression in formalin-fixed, paraffin-embedded prostate tumoursLiesel M FitzGerald, Kelsie Raspin, James R Marthick, et al.
European Journal of Human Genetics : EJHG|April 19, 2021
A 127 kb truncating deletion of PGRMC1 is a novel cause of X-linked isolated paediatric cataractJohanna L Jones, Mark A Corbett, Elise Yeaman, et al.
Pageof 4