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Mapping a shared genetic basis for neurodevelopmental disorders
Distinct neurodevelopmental disorders have a common genetic etiology that explains the high degree of comorbidity among these disorders. A recent study sought to identify copy number variants across five neurodevelopmental disorders, and detected an enrichment for chromosome 9p24.3 duplication encom...
Tallennettuna:
| Julkaisussa: | Genome Med |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5729609/ https://ncbi.nlm.nih.gov/pubmed/29241461 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-017-0503-4 |
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