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Whole exome sequencing in fetal structural abnormalities: experience of 8 cases

dc.contributor.authorAltunoglu, U.
dc.contributor.authorKalayci, T.
dc.contributor.authorKayserili, H.
dc.contributor.authorKalelioglu, I. H.
dc.date.accessioned2021-03-06T20:11:48Z
dc.date.available2021-03-06T20:11:48Z
dc.identifier.citationAltunoglu U., Kalayci T., Kalelioglu I. H. , Kayserili H., "Whole exome sequencing in fetal structural abnormalities: experience of 8 cases", 50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.166-167
dc.identifier.otherav_f92fff8e-9b11-4507-92dc-93662c0c0b17
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/163218
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.titleWhole exome sequencing in fetal structural abnormalities: experience of 8 cases
dc.typeBildiri
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume26
dc.contributor.firstauthorID154596


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