Ophthalmic Genetics,volume 22,issue 1  (03-2014)

Period of time: 2014年1期

Publisher: Informa Healthcare

Founded in: 1981

Total resources: 61

ISSN: 1381-6810

Subject: R77 Ophthalmology

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Ophthalmic Genetics,volume 22,issue 1

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Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomalies

By Lavanchy Laure,Munier Francis L.,Cousin Pascal,Gaide Anne-Claude,Thonney Francine,Schorderet Daniel F. in (2001)

Ophthalmic Genetics,volume 22,issue 1 , Vol. 22, Iss. 1, 2001-03 , pp. 1-10

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Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patients

By Bojinova Rossiana I.,Schorderet Daniel F.,Addor Marie-Claude,Gaide Anne-Claude,Thonney Francine,Pescia Graziano,Nenadov-Beck Maja,Balmer Aubin,Munier Francis L. in (2001)

Ophthalmic Genetics,volume 22,issue 1 , Vol. 22, Iss. 1, 2001-03 , pp. 11-18

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EFEMP1 is not associated with sporadic early onset drusen

By Sauer C.G.,White K.,Kellner U.,Rudolph G.,Jurklies B.,Pauleikhoff D.,Weber B.H.F. in (2001)

Ophthalmic Genetics,volume 22,issue 1 , Vol. 22, Iss. 1, 2001-03 , pp. 27-34

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Laboratory methods in ophthalmic genetics: obtaining DNA from patients

By Dickinson Joanne L.,Sale Michèle M.,Craig Jamie E.,Mackey David A. in (2001)

Ophthalmic Genetics,volume 22,issue 1 , Vol. 22, Iss. 1, 2001-03 , pp. 49-60

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