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Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion Syndrome
22q11.2DS is a chromosomal microdeletion that affects approximately 40–50 genes, and impacts various organs and systems throughout the body. Detection is typically achieved by fluorescence in-situ hybridization following diagnosis of one of the major features of the deletion or via chromosomal micro...
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| Publicado no: | J Dev Behav Pediatr |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4586411/ https://ncbi.nlm.nih.gov/pubmed/26372046 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/DBP.0000000000000210 |
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