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Phenotypic and Molecular Characterization of Cockayne Syndrome; A Spotlight to Mild Cases

dc.contributor.authorGunes, N.
dc.contributor.authorYesil, Gözde
dc.contributor.authorTuysuz, B.
dc.contributor.authorKubisch, C.
dc.contributor.authorLessel, D.
dc.contributor.authorAkyuz, E.
dc.date.accessioned2021-03-03T12:39:18Z
dc.date.available2021-03-03T12:39:18Z
dc.identifier.citationYesil G., Akyuz E., Gunes N., Lessel D., Kubisch C., Tuysuz B., "Phenotypic and Molecular Characterization of Cockayne Syndrome; A Spotlight to Mild Cases", 50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.406-407
dc.identifier.otherav_2f4d485c-73cb-4aec-b40d-3b19d486095e
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/36328
dc.language.isoeng
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.titlePhenotypic and Molecular Characterization of Cockayne Syndrome; A Spotlight to Mild Cases
dc.typeBildiri
dc.contributor.departmentBezmiâlem Vakıf Üniversitesi , ,
dc.identifier.volume26
dc.contributor.firstauthorID1043011


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