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Molecular Analysis of the Noggin (NOG) Gene in Holoprosencephaly Patients
Holoprosencephaly (HPE) is the most common structural anomaly of the human forebrain. Various genetic and teratogenic causes have been implicated in its pathogenesis. A recent report in mice described Noggin (NOG) as a candidate gene involved in the etiogenesis of microform HPE. Here, we present for...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3356444/ https://ncbi.nlm.nih.gov/pubmed/22503063 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2012.03.008 |
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