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Clinical and cytogenetic studies of two cases of Klinefelter syndrome with hereditary retinoblastoma and rhabdomyosarcoma.

dc.contributor.authorSengun, Z
dc.contributor.authorArelKilic, G
dc.contributor.authorDeBusscher, C
dc.contributor.authorOzbek, U
dc.contributor.authorSariban, E
dc.contributor.authorVamos, E
dc.contributor.authorBasaran, Seher
dc.contributor.authorAyan, I
dc.contributor.authorOgur, G
dc.date.accessioned2021-03-06T10:39:31Z
dc.date.available2021-03-06T10:39:31Z
dc.date.issued1996
dc.identifier.citationOgur G., Sengun Z., ArelKilic G., DeBusscher C., Basaran S., Ozbek U., Ayan I., Sariban E., Vamos E., "Clinical and cytogenetic studies of two cases of Klinefelter syndrome with hereditary retinoblastoma and rhabdomyosarcoma.", Cancer genetics and cytogenetics, cilt.89, ss.77-81, 1996
dc.identifier.issn0165-4608
dc.identifier.otherav_eb6f34c5-9b7d-4b5b-bd0e-b145234995aa
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/154610
dc.identifier.urihttps://doi.org/10.1016/0165-4608(96)00352-4
dc.description.abstractTwo children with Klinefelter syndrome (KS), one associated with bilateral hereditary retinoblastoma (RB) and the other with rhabdomyosarcoma (RMS) are reported, Both were boys and chromosomally mosaic for KS. The hereditary retinoblastoma case yielded 46,XY,del(13)(q12q14.2)/47, XXYc,del(13)(q12q14.2) in PHA-stimulated lymphocytes. The rhabdomyosarcoma case yielded 46,XY/47,XXYc in peripheral blood cells whereas tumor revealed trisomy 8, trisomy 7, and t(7;13)(q33;q32) in addition to 46,XY/47,XXYc mosaicism.
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectONKOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectOnkoloji
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.titleClinical and cytogenetic studies of two cases of Klinefelter syndrome with hereditary retinoblastoma and rhabdomyosarcoma.
dc.typeMakale
dc.relation.journalCancer genetics and cytogenetics
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume89
dc.identifier.issue1
dc.identifier.startpage77
dc.identifier.endpage81
dc.contributor.firstauthorID117700


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