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Changing Paradigms in Down Syndrome: The First International Conference of the Trisomy 21 Research Society
Down syndrome (DS) is the most common genetic cause of intellectual disability (ID) in humans with an incidence of ∼1:1,000 live births worldwide. It is caused by the presence of an extra copy of all or a segment of the long arm of human chromosome 21 (trisomy 21). People with DS present with a cons...
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| Publicado no: | Mol Syndromol |
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| Main Authors: | , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
S. Karger AG
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5109983/ https://ncbi.nlm.nih.gov/pubmed/27867340 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000449049 |
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