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FRA18C: a new aphidicolin‐inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage

Fragile sites are specific genomic loci that form gaps, constrictions and breaks on chromosomes exposed to replication stress conditions. In the father of a patient with Beckwith‐Wiedemann syndrome and a pure truncation of 18q22‐qter, a new aphidicolin‐sensitive fragile site on chromosome 18q22.2 (F...

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Detaylı Bibliyografya
Asıl Yazarlar: Debacker, Kim, Winnepenninckx, Birgitta, Ben‐Porat, Neta, FitzPatrick, David, Van Luijk, Rob, Scheers, Stefaan, Kerem, Batsheva, Kooy, R Frank
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Group 2007
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2597991/
https://ncbi.nlm.nih.gov/pubmed/17475918
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.044628
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