Haplotype Phasing and Inheritance of Copy Number Variants in Nuclear Families

DNA copy number variants (CNVs) that alter the copy number of a particular DNA segment in the genome play an important role in human phenotypic variability and disease susceptibility. A number of CNVs overlapping with genes have been shown to confer risk to a variety of human diseases thus highlight...

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Detalles Bibliográficos
Autores principales: Palta, Priit, Kaplinski, Lauris, Nagirnaja, Liina, Veidenberg, Andres, Möls, Märt, Nelis, Mari, Esko, Tõnu, Metspalu, Andres, Laan, Maris, Remm, Maido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390228/
https://www.ncbi.nlm.nih.gov/pubmed/25853576
http://dx.doi.org/10.1371/journal.pone.0122713

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390228/
https://www.ncbi.nlm.nih.gov/pubmed/25853576
http://dx.doi.org/10.1371/journal.pone.0122713

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