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Cornelia de Lange syndrome, cohesin, and beyond
Cornelia de Lange syndrome (CdLS) (OMIM #122470, #300590 and #610759) is a dominant genetic disorder with multiple organ system abnormalities which is classically characterized by typical facial features, growth and mental retardation, upper limb defects, hirsutism, gastrointestinal and other viscer...
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| Glavni autori: | , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2009
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2853897/ https://ncbi.nlm.nih.gov/pubmed/19793304 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2009.01271.x |
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