Show simple item record

dc.contributor.authorKurtulgan, H.K.
dc.contributor.authorÖzer, L.
dc.contributor.authorYildirim, M.E.
dc.contributor.authorÜnsal, E.
dc.contributor.authorAktuna, S.
dc.contributor.authorBaltaci, V.
dc.contributor.authorAkkuş, N.
dc.contributor.authorSezgin, I.
dc.date.accessioned2021-12-21T08:41:38Z
dc.date.available2021-12-21T08:41:38Z
dc.date.issued2015
dc.identifier.issn17558166
dc.identifier.urihttps://doi.org/10.1186/s13039-015-0195-7
dc.identifier.urihttp://dspace.yeniyuzyil.edu.tr:8080/xmlui/handle/20.500.12629/1477
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.publisherBioMed Central Ltd.
dc.rightsAll Open Access, Gold, Green
dc.titleRecombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion
dc.typeArticle
dc.relation.journalMolecular Cytogenetics
dc.identifier.issue1
dc.identifier.volume8
dc.identifier.doi10.1186/s13039-015-0195-7
dc.relation.issue1
dc.relation.volume8


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record