Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants

BACKGROUND: Copy number variations (CNVs) having no (obvious) clinical effects were rediscovered as major part of human genome in 2004. However, for every cytogeneticist microscopically visible harmless CNVs (CG-CNVs) are well known since decades. Harmless CG-CNVs can be present as heterochromatic o...

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Detalles Bibliográficos
Autor principal: Liehr, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724132/
https://www.ncbi.nlm.nih.gov/pubmed/26807150
http://dx.doi.org/10.1186/s13039-016-0216-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724132/
https://www.ncbi.nlm.nih.gov/pubmed/26807150
http://dx.doi.org/10.1186/s13039-016-0216-1

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