dc.contributor.author | Kurtulgan, H.K. | |
dc.contributor.author | Özer, L. | |
dc.contributor.author | Yildirim, M.E. | |
dc.contributor.author | Ünsal, E. | |
dc.contributor.author | Aktuna, S. | |
dc.contributor.author | Baltaci, V. | |
dc.contributor.author | Akkuş, N. | |
dc.contributor.author | Sezgin, I. | |
dc.date.accessioned | 2021-12-21T08:41:38Z | |
dc.date.available | 2021-12-21T08:41:38Z | |
dc.date.issued | 2015 | |
dc.identifier.issn | 17558166 | |
dc.identifier.uri | https://doi.org/10.1186/s13039-015-0195-7 | |
dc.identifier.uri | http://dspace.yeniyuzyil.edu.tr:8080/xmlui/handle/20.500.12629/1477 | |
dc.description.abstract | Background: 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.iso | English | |
dc.publisher | BioMed Central Ltd. | |
dc.rights | All Open Access, Gold, Green | |
dc.title | Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion | |
dc.type | Article | |
dc.relation.journal | Molecular Cytogenetics | |
dc.identifier.issue | 1 | |
dc.identifier.volume | 8 | |
dc.identifier.doi | 10.1186/s13039-015-0195-7 | |
dc.relation.issue | 1 | |
dc.relation.volume | 8 | |