Basit öğe kaydını göster

DE-NOVO X/X TRANSLOCATION IN A PATIENT WITH SECONDARY AMENORRHEA

dc.contributor.authorSILAHTAROGLU, AN
dc.contributor.authorCENANI, A
dc.contributor.authorHACIHANEFIOGLU, S
dc.contributor.authorDEVIREN, A
dc.contributor.authorTOPCUOGLU, D
dc.contributor.authorTARKAN, Y
dc.date.accessioned2021-03-03T12:07:46Z
dc.date.available2021-03-03T12:07:46Z
dc.date.issued1995
dc.identifier.citationTARKAN Y., HACIHANEFIOGLU S., SILAHTAROGLU A., DEVIREN A., TOPCUOGLU D., CENANI A., "DE-NOVO X/X TRANSLOCATION IN A PATIENT WITH SECONDARY AMENORRHEA", HEREDITAS, cilt.122, sa.1, ss.19-23, 1995
dc.identifier.issn0018-0661
dc.identifier.otherav_2c11c25f-6945-4f57-8b7b-6ad210af8a0b
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/34352
dc.identifier.urihttps://doi.org/10.1111/j.1601-5223.1995.00019.x
dc.description.abstractA 46,X,t(X;X) (qter --> p22::p22 --> qter) karyotype was found in the chromosome analysis of a 22 years old female patient with secondary amenorrhea. Further analysis with fluorescence in situ hybridization indicated that the marker chromosome had one active and one inactive centromere originating from the X chromosome. RBG-banding showed that the derivative X chromosome was preferentially inactivated in cultured lymphocytes.
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleDE-NOVO X/X TRANSLOCATION IN A PATIENT WITH SECONDARY AMENORRHEA
dc.typeMakale
dc.relation.journalHEREDITAS
dc.contributor.department, ,
dc.identifier.volume122
dc.identifier.issue1
dc.identifier.startpage19
dc.identifier.endpage23
dc.contributor.firstauthorID115900


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster