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Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder
BACKGROUND: Obsessive-compulsive disorder (OCD) is a clinically and etiologically heterogeneous syndrome. The high frequency of obsessive-compulsive symptoms reported in subjects with the 22q11.2 deletion syndrome (DiGeorge/velocardiofacial syndrome) or Prader-Willi syndrome (15q11-13 deletion of th...
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| Autors principals: | , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2909937/ https://ncbi.nlm.nih.gov/pubmed/20565924 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-100 |
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