The Cytoscan HD Array in the Diagnosis of Neurodevelopmental Disorders

Submicroscopic chromosomal copy number variations (CNVs), such as deletions and duplications, account for about 15–20% of patients affected with developmental delay, intellectual disability, multiple congenital anomalies, and autism spectrum disorder. Most of CNVs are de novo or inherited rearrangem...

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Detalles Bibliográficos
Autores principales: Scionti, Francesca, Di Martino, Maria Teresa, Pensabene, Licia, Bruni, Valentina, Concolino, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164295/
https://www.ncbi.nlm.nih.gov/pubmed/30223503
http://dx.doi.org/10.3390/ht7030028

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164295/
https://www.ncbi.nlm.nih.gov/pubmed/30223503
http://dx.doi.org/10.3390/ht7030028

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