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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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| I publikationen: | Sci Rep |
|---|---|
| Huvudupphovsmän: | , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Nature Publishing Group UK
2021
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| Ämnen: | |
| Länkar: | 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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