Chromosomal microarray analysis, or comparative genomic hybridization: A high throughput approach

Pathological copy number variants (CNVs) and point mutations are major genetic causes of hundreds of disorders. Comparative genomic hybridization (CGH) also known as chromosomal microarray analysis (CMA) is the best available tool to detect copy number variations in chromosomal make up. We have opti...

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Detalles Bibliográficos
Autores principales: Haeri, Mohammad, Gelowani, Violet, Beaudet, Arthur L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Biochemistry, Genetics and Molecular Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707176/
https://www.ncbi.nlm.nih.gov/pubmed/26862485
http://dx.doi.org/10.1016/j.mex.2015.11.005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707176/
https://www.ncbi.nlm.nih.gov/pubmed/26862485
http://dx.doi.org/10.1016/j.mex.2015.11.005

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