Cargando…
Genomic Copy Number Variations in the Autism Clinic—Work in Progress
The development of advanced technology for microarray-based chromosomal studies helped discover increased prevalence of genomic copy number variants (CNVs) in individuals with autism spectrum disorder (ASD). Chromosomal microarray analysis (CMA) is now an important tool for clinical investigations i...
Autor principal: | Velinov, Milen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389619/ https://www.ncbi.nlm.nih.gov/pubmed/30837845 http://dx.doi.org/10.3389/fncel.2019.00057 |
Ejemplares similares
-
Potential Value of Genomic Copy Number Variations in Schizophrenia
por: Zhuo, Chuanjun, et al.
Publicado: (2017) -
FMR1 and Autism, an Intriguing Connection Revisited
por: Fyke, William, et al.
Publicado: (2021) -
Copy number variations independently induce autism spectrum disorder
por: Yingjun, Xie, et al.
Publicado: (2017) -
Large mosaic copy number variations confer autism risk
por: Sherman, Maxwell A., et al.
Publicado: (2021) -
Copy number variations in Japanese children with autism spectrum disorder
por: Sakamoto, Yui, et al.
Publicado: (2021)