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...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2018-09-01
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| Series: | High-Throughput |
| Subjects: | |
| Online Access: | http://www.mdpi.com/2571-5135/7/3/28 |