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Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies
Chromosomal microarray (CMA) testing, used to identify DNA copy number variations (CNVs), has helped advance knowledge about genetics of human neurodevelopmental disease and congenital anomalies. It has aided in discovering new CNV syndromes and uncovering disease genes. It has discovered CNVs that...
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| Publicat a: | J Pediatr Genet |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Georg Thieme Verlag KG
2017
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| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5288005/ https://ncbi.nlm.nih.gov/pubmed/28180026 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0036-1584306 |
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