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A rarely seen 47,XXY/46,XX mosaicism of Klinefelter syndrome: Case report

dc.contributor.authorYigin, A. Kalayci
dc.contributor.authorSeven, M.
dc.contributor.authorGumus, U.
dc.date.accessioned2021-03-04T15:06:24Z
dc.date.available2021-03-04T15:06:24Z
dc.identifier.citationYigin A. K. , Gumus U., Seven M., "A rarely seen 47,XXY/46,XX mosaicism of Klinefelter syndrome: Case report", 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.1020
dc.identifier.otherav_85044a02-5ca6-443f-8341-4d232151173b
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/90462
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTemel Bilimler
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.titleA rarely seen 47,XXY/46,XX mosaicism of Klinefelter syndrome: Case report
dc.typeBildiri
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume27
dc.contributor.firstauthorID156350


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