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Ophthalmic Genetics|July 17, 2004
Fluorine-18 fluorodeoxyglucose positron emission tomography (PET) to detect vital retinoblastoma in the eye: preliminary experienceA C Moll, O S Hoekstra, S M Imhof, et al.Ophthalmic Genetics|July 17, 2004
Activity of topotecan in retinoblastomaGuillermo L Chantada, Adriana C Fandiño, Sandra J Casak, et al.Ophthalmic Genetics|July 17, 2004
A second primary tumor in a patient with retinomaLindy-Anne Korswagen, Annette C Moll, Saskia M Imhof, et al.Ophthalmic Genetics|December 29, 2004
Mutation analysis of KIF21A in congenital fibrosis of the extraocular muscles (CFEOM) patientsLeila Tiab, Violaine d'Allèves Manzi, François-Xavier Borruat, et al.Ophthalmic Genetics|December 29, 2004
Fundus features of a case of neurocutaneous melanosisHayyam Kiratli, Afsun SahinOphthalmic Genetics|March 23, 2002
Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish familySerap Ozden, Füsun Düzcan, Bernd Wollnik, et al.Ophthalmic Genetics|March 23, 2002
A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome: differential role of the polyalanine tract in the development of the ovary and the eyelidKenjiro Kosaki, Tsutomu Ogata, Rika Kosaki, et al.Ophthalmic Genetics|June 1, 1994
Autosomal dominant retinitis pigmentosa. A mutation in codon 181 (Glu-->Lys) of the rhodopsin gene in a Japanese familyM Saga, Y Mashima, K Akeo, et al.Ophthalmic Genetics|June 1, 1994
Genetic isolate and preserved para-arteriole retinal pigment epitheliumA Piantanida, P Nucci, R BrancatoPageof 185