Caricamento...

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...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Debacker, Kim, Winnepenninckx, Birgitta, Ben‐Porat, Neta, FitzPatrick, David, Van Luijk, Rob, Scheers, Stefaan, Kerem, Batsheva, Kooy, R Frank
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMJ Group 2007
Soggetti:
Accesso online: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
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !