Lataa...
Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome
22q11.2 Deletion Syndrome (22q11.2DS) is a common microdeletion syndrome with congenital and late-onset features. Testing for the genomic content of copy number variations (CNVs) may help elucidate the 22q11.2 deletion mechanism and the variable clinical expression of the syndrome including the high...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2008
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2638574/ https://ncbi.nlm.nih.gov/pubmed/18806272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn307 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|