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dc.contributor.authorPercin, EF
dc.contributor.authorArici, K
dc.contributor.authorHorsford, DJ
dc.contributor.authorKocak-Altintas, A
dc.contributor.authorAkarsu, AN
dc.contributor.authorMcInnes, RR
dc.contributor.authorSarfarazi, M
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:25:42Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:25:42Z
dc.date.issued1999
dc.identifier.issn0002-9297
dc.identifier.urihttps://hdl.handle.net/20.500.12418/11734
dc.descriptionWOS: 000082879800095en_US
dc.description.abstracten_US
dc.language.isoengen_US
dc.publisherUNIV CHICAGO PRESSen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleA new locus for autosomal recessive Congenital Microphthalmia maps to 14q24.3 and caused by a homozygous mutation in the CHX10 gene.en_US
dc.typeconferenceObjecten_US
dc.relation.journalAMERICAN JOURNAL OF HUMAN GENETICSen_US
dc.contributor.departmentUniv Connecticut, Ctr Hlth, Farmington, CT USA -- Cumhuriyet Univ, Sivas, Turkey -- Hosp Sick Children, Toronto, ON M5G 1X8, Canada -- Ankara Hosp, Dept Ophthalmol, Ankara, Turkey -- Hacettepe Univ, DNA Cell Bank, Ankara, Turkeyen_US
dc.contributor.authorIDPercin, Ferda -- 0000-0001-9317-8155en_US
dc.identifier.volume65en_US
dc.identifier.issue4en_US
dc.identifier.endpageA19en_US
dc.identifier.startpageA19en_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US


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