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Whole Exome Sequence Analyses In A Consanguıneous Famıly Wıth Affected Dizygotic Twins Reveal A Novel SEPN1 Variant Associated With Multiminicore Disease

dc.contributor.authorBayrak, Ayşe Evrim
dc.contributor.authorOflazer, Piraye
dc.contributor.authorTuncer Kılınç, Feyza Nur
dc.contributor.authorSalman Yılmaz, S.
dc.contributor.authorVural, Burçak
dc.contributor.authorSarı Tunel, Fatma
dc.date.accessioned2022-02-18T09:18:21Z
dc.date.available2022-02-18T09:18:21Z
dc.identifier.citationSarı Tunel F., Tuncer Kılınç F. N. , Bayrak A. E. , Salman Yılmaz S., Oflazer P., Vural B., "Whole Exome Sequence Analyses In A Consanguıneous Famıly Wıth Affected Dizygotic Twins Reveal A Novel SEPN1 Variant Associated With Multiminicore Disease", 13th Balkan Congress of Human Genetics, Edirne, Türkiye, 17 - 20 Nisan 2019, ss.76
dc.identifier.othervv_1032021
dc.identifier.otherav_2da14d23-a3de-4f35-91b6-71b06a77d724
dc.identifier.urihttp://hdl.handle.net/20.500.12627/176937
dc.language.isoeng
dc.subjectGENETİK VE HAYAT
dc.subjectGenetics
dc.subjectGenetics (clinical)
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectKlinik Tıp (MED)
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectKlinik Tıp
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTıbbi Genetik
dc.titleWhole Exome Sequence Analyses In A Consanguıneous Famıly Wıth Affected Dizygotic Twins Reveal A Novel SEPN1 Variant Associated With Multiminicore Disease
dc.typeBildiri
dc.contributor.departmentİstanbul Üniversitesi , Aziz Sancar Deneysel Tıp Araştırma Enstitüsü , Genetik Ana Bilim Dalı
dc.contributor.firstauthorID3066569


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