Deficiencies in the region syntenic to human 21q22.3 causes cognitive deficits in mice

Copy-number variation in the human genome can be disease-causing or phenotypically neutral. This type of genetic rearrangement associated with human chromosome 21 (Hsa21) underlies partial Monosomy 21 and Trisomy 21. Mental retardation is a major clinical manifestation of partial Monosomy 21. To mod...

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Main Authors: Yu, Tao, Clapcote, Steven J., Li, Zhongyou, Liu, Chunhong, Pao, Annie, Bechard, Allison R., Carattini-Rivera, Sandra, Matsui, Sei-Ichi, Roder, John C., Baldini, Antonio, Mobley, William C., Bradley, Allan, Yu, Y. Eugene
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3023176/
https://ncbi.nlm.nih.gov/pubmed/20512340
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00335-010-9262-x
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