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A telehealth approach to improving clinical trial access for infants with tuberous sclerosis complex
BACKGROUND: Research in rare genetic syndromes associated with ASD is often hampered by the wide geographic distribution of families and the presence of medical comorbidities, such as epilepsy, that may preclude travel to clinical sites. These challenges can limit the sample size and generalizabilit...
Guardat en:
| Publicat a: | J Neurodev Disord |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6977334/ https://ncbi.nlm.nih.gov/pubmed/31969108 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-019-9302-0 |
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