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Genetic Enhancement of Limb Defects in a Mouse Model of Cornelia de Lange Syndrome
Cornelia de Lange Syndrome (CdLS) is characterized by a wide variety of structural and functional abnormalities in almost every organ system of the body. CdLS is now known to be caused by mutations that disrupt the function of the cohesin complex or its regulators, and studies of animal models and c...
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| Publicado no: | Am J Med Genet C Semin Med Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4921392/ https://ncbi.nlm.nih.gov/pubmed/27120109 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.c.31491 |
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