Ophthalmic Genetics,volume 24,issue 4  (12-2014)

Period of time: 2014年4期

Publisher: Informa Healthcare

Founded in: 1981

Total resources: 61

ISSN: 1381-6810

Subject: R77 Ophthalmology

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Ophthalmic Genetics,volume 24,issue 4

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Phenotypic variability in three carriers from a family with choroideremia and a frameshift mutation 1388delCCinsG in the REP-1 gene

By Rudolph Günther,Preising Markus,Kalpadakis Petros,Haritoglou Christos,Lang Gabriele E.,Lorenz Birgit in (2003)

Ophthalmic Genetics,volume 24,issue 4 , Vol. 24, Iss. 4, 2003-12 , pp. 203-214 (12)

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Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes

By Andréasson Sten,Breuer Debra K.,Eksandh Louise,Ponjavic Vesna,Frennesson Christina,Hiriyanna Suja,Filippova Elena,Yashar Beverly M.,Swaroop Anand in (2003)

Ophthalmic Genetics,volume 24,issue 4 , Vol. 24, Iss. 4, 2003-12 , pp. 215-223 (9)

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Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene

By Gränse Lotta,Bergstrand Ingar,Thiselton Dawn,Ponjavic Vesna,Heijl Anders,Votruba Marcela,Andréasson Sten in (2003)

Ophthalmic Genetics,volume 24,issue 4 , Vol. 24, Iss. 4, 2003-12 , pp. 233-245 (13)

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Retinopathy of incontinentia pigmenti: a case report with thirteen years follow-up

By Cates Carolyn A.,Dandekar Samantha S.,Flanagan Declan W.,Moore Anthony T. in (2003)

Ophthalmic Genetics,volume 24,issue 4 , Vol. 24, Iss. 4, 2003-12 , pp. 247-252 (6)

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