| dc.contributor.author | Güneş S. | |
| dc.contributor.author | Kara N. | |
| dc.contributor.author | Sürücü B. | |
| dc.contributor.author | Ökten G. | |
| dc.contributor.author | Yiğit S. | |
| dc.contributor.author | Sezer Ö. | |
| dc.date.accessioned | 2020-06-21T09:24:45Z | |
| dc.date.available | 2020-06-21T09:24:45Z | |
| dc.date.issued | 2008 | |
| dc.identifier.issn | 1300-0292 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/3865 | |
| dc.description.abstract | Turner's syndrome is one of the most common chromosomal aneuploidy disorders. Turner's syndrome occurs in 1 in 4000 live-born girls and approximately 5 to 10 percent of them have mosaic isochromosome 45,X/46,X,i(Xq). Turner's syndrome is associated with reduced adult height and with gonadal dysgenesis, leading to insufficient circulating levels of female sex steroids and to infertility. In this study, we presented 18 year-old two girls having complaints of primary amenorrhea with mosaic 46,X,i(X)(qter?q10 | en_US |
| dc.language.iso | tur | en_US |
| dc.publisher | Turkiye Klinikleri | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Isochromosomes | en_US |
| dc.subject | Turner syndrome | en_US |
| dc.title | Two Turner syndrome patients with the mosaic 45,X/46,X,i(Xq) karyotype: Case report [45,X/46,X,i(Xq) karyotipe sahip i?ki mozaik Turner sendromu olgusu] | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 28 | en_US |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.startpage | 236 | en_US |
| dc.identifier.endpage | 238 | en_US |
| dc.relation.journal | Turkiye Klinikleri Journal of Medical Sciences | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
