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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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| Asıl Yazarlar: | , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2006
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| Konular: | |
| Online Erişim: | 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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