The Human Genome Puzzle – the Role of Copy Number Variation in Somatic Mosaicism

The discovery of copy number variations (CNV) in the human genome opened new perspectives in the study of the genetic causes of inherited disorders and the etiology of common diseases. Differently patterned instances of somatic mosaicism in CNV regions have been shown to be present in monozygotic tw...

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Detalles Bibliográficos
Autores principales: Mkrtchyan, Hasmik, Gross, Madeleine, Hinreiner, Sophie, Polytiko, Anna, Manvelyan, Marina, Mrasek, Kristin, Kosyakova, Nadezda, Ewers, Elisabeth, Nelle, Heike, Liehr, Thomas, Bhatt, Samarth, Thoma, Karen, Gebhart, Erich, Wilhelm, Sylvia, Fahsold, Raimund, Volleth, Marianne, Weise, Anja
Formato: Texto
Lenguaje:English
Publicado: Bentham Science Publishers Ltd. 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018723/
https://www.ncbi.nlm.nih.gov/pubmed/21358987
http://dx.doi.org/10.2174/138920210793176047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018723/
https://www.ncbi.nlm.nih.gov/pubmed/21358987
http://dx.doi.org/10.2174/138920210793176047

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