A new locus for autosomal recessive Congenital Microphthalmia maps to 14q24.3 and caused by a homozygous mutation in the CHX10 gene.
dc.contributor.author | Percin, EF | |
dc.contributor.author | Arici, K | |
dc.contributor.author | Horsford, DJ | |
dc.contributor.author | Kocak-Altintas, A | |
dc.contributor.author | Akarsu, AN | |
dc.contributor.author | McInnes, RR | |
dc.contributor.author | Sarfarazi, M | |
dc.date.accessioned | 2019-07-27T12:10:23Z | |
dc.date.accessioned | 2019-07-28T10:25:42Z | |
dc.date.available | 2019-07-27T12:10:23Z | |
dc.date.available | 2019-07-28T10:25:42Z | |
dc.date.issued | 1999 | |
dc.identifier.issn | 0002-9297 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12418/11734 | |
dc.description | WOS: 000082879800095 | en_US |
dc.description.abstract | … | en_US |
dc.language.iso | eng | en_US |
dc.publisher | UNIV CHICAGO PRESS | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.title | A new locus for autosomal recessive Congenital Microphthalmia maps to 14q24.3 and caused by a homozygous mutation in the CHX10 gene. | en_US |
dc.type | conferenceObject | en_US |
dc.relation.journal | AMERICAN JOURNAL OF HUMAN GENETICS | en_US |
dc.contributor.department | Univ 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, Turkey | en_US |
dc.contributor.authorID | Percin, Ferda -- 0000-0001-9317-8155 | en_US |
dc.identifier.volume | 65 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.endpage | A19 | en_US |
dc.identifier.startpage | A19 | en_US |
dc.relation.publicationcategory | Konferans Öğesi - Uluslararası - Kurum Öğretim Elemanı | en_US |
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