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The prevalance of 22q11.2 deletion in children with congenital heart disease and dismorphic features

dc.contributor.authorYilmaz, Elif
dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorOztunc, Funda
dc.contributor.authorKaya, Kaya
dc.contributor.authorCankaya, Tufan
dc.date.accessioned2021-03-03T15:57:31Z
dc.date.available2021-03-03T15:57:31Z
dc.identifier.citationKaya K., Cankaya T., Yilmaz E., Oztunc F., Tuysuz B., "The prevalance of 22q11.2 deletion in children with congenital heart disease and dismorphic features", 6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.77
dc.identifier.otherav_41a3bbe8-53fe-4dcd-b2a9-7dc6b0e92a41
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/47871
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.titleThe prevalance of 22q11.2 deletion in children with congenital heart disease and dismorphic features
dc.typeBildiri
dc.contributor.department, ,
dc.identifier.volume15
dc.contributor.firstauthorID133367


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