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Novel evidence of association with NSCL/P was shown for SNPs in FOXF2 gene in an Asian population
BACKGROUND: The forkhead box F2 gene (FOXF2) located in chromosome 6p25.3 has been shown to play a crucial role in palatal development in mouse and rat models. To date, no evidence of linkage or association has been reported for this gene in humans with oral clefts. METHODS: Allelic transmission dis...
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| Publicat a: | Birth Defects Res A Clin Mol Teratol |
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| Autors principals: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5180447/ https://ncbi.nlm.nih.gov/pubmed/26278207 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.23413 |
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