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Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome
22q11 Deletion syndrome (22q11DS) is a common microdeletion syndrome with variable expression, including congenital and later onset conditions such as schizophrenia. Most studies indicate that expression does not appear to be related to length of the deletion but there is limited information on the...
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| 主要な著者: | , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2006
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3139629/ https://ncbi.nlm.nih.gov/pubmed/17028864 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-006-0242-x |
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