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On the Molecular Etiology of Cornelia de Lange Syndrome
Cornelia de Lange syndrome (CdLS) is genetically heterogeneous and is usually sporadic, occurring approximately once per ten thousand births. CdLS individuals display diverse and variable deficits in growth, mental development, limbs and organs. In the past few years it has been shown that CdLS is c...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2009
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2733214/ https://ncbi.nlm.nih.gov/pubmed/19154515 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1749-6632.2008.03450.x |
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