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Chromosomal instability in patients with Fanconi anemia from Serbia

Background/Aim. Fanconi anemia (FA) is a rare hereditary disease in a heterogeneous group of syndromes, so-called chromosome breakage disorders. Specific hypersensitivity of its cells to chemical agents, such as diepoxybutane (DEB), was used as a part of screening among patients with cli...

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Detaylı Bibliyografya
Asıl Yazarlar: Ćirković Sanja, Guć-Šćekić Marija, Vujić Dragana, Mićić Dragan, Škorić Dejan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Ministry of Defence of the Republic of Serbia, University of Defence, Belgrade 2014-01-01
Seri Bilgileri:Vojnosanitetski Pregled
Konular:
Online Erişim:http://www.doiserbia.nb.rs/img/doi/0042-8450/2014/0042-84501404368C.pdf
Etiketler: Etiketle
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