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Ophthalmic Genetics|January 3, 2001
Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN)W S Oetting, C M Armstrong, A M Holleschau, et al.Ophthalmic Genetics|July 13, 2001
Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage disequilibrium analysisT L Young, L D Atwood, S M Ronan, et al.Ophthalmic Genetics|July 13, 2001
Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 geneL Eksandh, B Bakall, B Bauer, et al.Ophthalmic Genetics|February 5, 2003
TGFBI gene transcript is transforming growth factor-beta1-responsive and cell density-dependent in a human corneal epithelial cell lineMing Wang, Francis Munier, Kaoru Araki-Saski, et al.Ophthalmic Genetics|June 6, 2003
A novel syndrome of congenital lid and punctal anomalies, corneal and chorioretinal dystrophyThomas K M Lee, Marc Hébert, Ian M MacDonaldOphthalmic Genetics|June 6, 2003
Congenital cystic eye: recurrence after initial surgical removalRichard M Robb, Douglas C AnthonyOphthalmic Genetics|June 1, 1994
Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch familyL I van den Born, M J van Schooneveld, L A de Jong, et al.Ophthalmic Genetics|September 27, 2007
Screening of the USH1G gene among Spanish patients with Usher syndrome. Lack of mutations and evidence of a minor role in the pathogenesis of the syndromeElena Aller, Teresa Jaijo, Magdalena Beneyto, et al.Ophthalmic Genetics|September 27, 2007
Retinal dysfunction in carriers of bardet-biedl syndromeLinda S Kim, Gerald A Fishman, William H Seiple, et al.Pageof 185