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Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms
BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is the most common micro-deletion syndrome. The associated 22q11.2 deletion conveys the strongest known molecular risk for schizophrenia. Neurodevelopmental phenotypes, including intellectual disability, are also prominent though variable in severity...
Gorde:
| Argitaratua izan da: | J Neurodev Disord |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2015
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4487986/ https://ncbi.nlm.nih.gov/pubmed/26137170 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-015-9113-x |
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