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Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair

Recurrent submicroscopic genomic copy number changes are the result of nonallelic homologous recombination (NAHR). Nonrecurrent aberrations, however, can result from different nonexclusive recombination-repair mechanisms. We previously described small microduplications at Xq28 containing MECP2 in fo...

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Detalhes bibliográficos
Main Authors: Bauters, Marijke, Van Esch, Hilde, Friez, Michael J., Boespflug-Tanguy, Odile, Zenker, Martin, Vianna-Morgante, Angela M., Rosenberg, Carla, Ignatius, Jaakko, Raynaud, Martine, Hollanders, Karen, Govaerts, Karen, Vandenreijt, Kris, Niel, Florence, Blanc, Pierre, Stevenson, Roger E., Fryns, Jean-Pierre, Marynen, Peter, Schwartz, Charles E., Froyen, Guy
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2008
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2413152/
https://ncbi.nlm.nih.gov/pubmed/18385275
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.075903.107
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