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dc.contributor.authorKurtulgan, Hande Kucuk
dc.contributor.authorOzer, Leyla
dc.contributor.authorYildirim, Malik Ejder
dc.contributor.authorUnsal, Evrim
dc.contributor.authorAktuna, Suleyman
dc.contributor.authorBaltaci, Volkan
dc.contributor.authorAkkus, Nejmiye
dc.contributor.authorSezgin, Ilhan
dc.date.accessioned2021-12-21T08:46:35Z
dc.date.available2021-12-21T08:46:35Z
dc.date.issued2015
dc.identifier.issn1755-8166
dc.identifier.urihttps://doi.org/10.1186/s13039-015-0195-7
dc.identifier.urihttp://dspace.yeniyuzyil.edu.tr:8080/xmlui/handle/20.500.12629/2044
dc.description.abstractBackground: 14q duplications caused by parental pericentric inversion of chromosome 14 are rarely reported and no clear genotype-phenotype correlation has been determined yet. Case Presentation: Here we reported a 7 years old female patient with recombina
dc.language.isoEnglish
dc.publisherBıomed Central Ltd
dc.rightsgold, Green Published
dc.titleRecombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion
dc.typeArticle
dc.relation.journalMolecular Cytogenetıcs
dc.identifier.volume8
dc.identifier.doi10.1186/s13039-015-0195-7
dc.relation.volume8


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