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Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability
Chromosomal microarray (CMA) analysis for discovery of copy number variants (CNVs) is now recommended as a first-line diagnostic tool in patients with unexplained developmental delay/intellectual disability (DD/ID) and autism spectrum disorders. In this study, we present the results of CMA analysis...
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| 發表在: | J Pediatr Genet |
|---|---|
| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Georg Thieme Verlag KG
2019
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| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6375720/ https://ncbi.nlm.nih.gov/pubmed/30775046 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0038-1676583 |
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