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Molecular Vision|June 17, 2011
A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa casesElsebet Ostergaard, Morten Duno, Mustafa Batbayli, et al.Ophthalmic Genetics|April 13, 2005
Hereditary high hypermetropia in the Faroe IslandsJosefine Fuchs, Kári Holm, Kaj Vilhelmsen, et al.Journal of Glaucoma|August 3, 2021
Prevalence of Open-angle Glaucoma in the Faroese PopulationElin Holm, Malan Holm, Kaj Vilhelmsen, et al.American Journal of Human Genetics|February 12, 2013
Mutations in c10orf11, a melanocyte-differentiation gene, cause autosomal-recessive albinismKaren Grønskov, Christopher M Dooley, Elsebet Østergaard, et al.American Journal of Human Genetics|March 15, 2011
Autosomal-recessive posterior microphthalmos is caused by mutations in PRSS56, a gene encoding a trypsin-like serine proteaseAndreas Gal, Isabella Rau, Leila El Matri, et al.Pageof 1