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Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm(†)

The constitutional t(11;22) is the most frequent recurrent non-Robertsonian translocation in humans, the breakpoints of which are located within palindromic AT-rich repeats on 11q23 and 22q11 (PATRR11 and PATRR22). Genetic variation of the PATRR11 was found to affect de novo t(11;22) translocation f...

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Detalhes bibliográficos
Main Authors: Tong, Maoqing, Kato, Takema, Yamada, Kouji, Inagaki, Hidehito, Kogo, Hiroshi, Ohye, Tamae, Tsutsumi, Makiko, Wang, Jieru, Emanuel, Beverly S., Kurahashi, Hiroki
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2883341/
https://ncbi.nlm.nih.gov/pubmed/20392709
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq150
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