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Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience
Chromosomal microarray analysis (CMA) is now established as the first-tier cytogenetic diagnostic test for fast and accurate detection of chromosomal abnormalities in patients with developmental delay/intellectual disability (DD/ID), multiple congenital anomalies (MCA), and autism spectrum disorders...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley Periodicals, Inc.
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3960059/ https://ncbi.nlm.nih.gov/pubmed/24689080 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.57 |
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