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Circulation|March 21, 2007
Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limbRussell H Mellor, Glen Brice, Anthony W B Stanton, et al.Human Genetics|June 20, 2002
Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucomaTin Aung, Louise Ocaka, Neil D Ebenezer, et al.Human Genetics|May 21, 2005
Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutationsCarolyn Sholto-Douglas-Vernon, Rachel Bell, Glen Brice, et al.Investigative Ophthalmology & Visual Science|July 27, 2005
Clinical features and course of patients with glaucoma with the E50K mutation in the optineurin geneTin Aung, Tayebeh Rezaie, Koji Okada, et al.Human Mutation|October 18, 2012
FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database updateKristiana Gordon, Sarah L Spiden, Fiona C Connell, et al.Science (New York, N.Y.)|February 9, 2002
Adult-onset primary open-angle glaucoma caused by mutations in optineurinTayebeh Rezaie, Anne Child, Roger Hitchings, et al.Journal of Medical Genetics|January 27, 2011
Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotypePia Ostergaard, Michael A Simpson, Glen Brice, et al.Circulation Research|February 16, 2013
Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedemaKristiana Gordon, Dörte Schulte, Glen Brice, et al.Investigative Ophthalmology & Visual Science|May 27, 2003
Novel anterior segment phenotypes resulting from forkhead gene alterations: evidence for cross-species conservation of functionOrdan J Lehmann, Stephen Tuft, Glen Brice, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 4, 2006
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypesFaisal Idrees, Agnes Bloch-Zupan, Samantha L Free, et al.Pageof 4