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Identification of a Van der Woude Syndrome mutation in the cleft palate 1 mutant mouse
Mutations in Interferon Regulatory Factor 6 (IRF6) have been identified in two human allelic syndromes with cleft lip and/or palate: Van der Woude (VWS) and Popliteal Pterygia (PPS) Syndromes. Furthermore, common IRF6 haplotypes and single nucleotide polymorphisms (SNP) alleles are strongly associat...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3117396/ https://ncbi.nlm.nih.gov/pubmed/20196077 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvg.20618 |
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