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Comorbidities associated with genetic abnormalities in children with intellectual disability
Intellectual disability (ID) has emerged as the commonest manifestation of underlying genomic abnormalities. Given that molecular genetic tests for diagnosis of ID usually require high costs and yield relatively low diagnostic rates, identification of additional phenotypes or comorbidities may incre...
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| 出版年: | Sci Rep |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group UK
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7985145/ https://ncbi.nlm.nih.gov/pubmed/33753861 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-86131-3 |
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