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Candidate gene analyses of 3-dimensional dentoalveolar phenotypes in subjects with malocclusion
INTRODUCTION: Genetic studies of malocclusion etiology have identified 4 deleterious mutations in genes, DUSP6, ARHGAP21, FGF23, and ADAMTS1 in familial Class III cases. Although these variants may have large impacts on Class III phenotypic expression, their low frequency (<1%) makes them unlikel...
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| Τόπος έκδοσης: | Am J Orthod Dentofacial Orthop |
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| Κύριοι συγγραφείς: | , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5358674/ https://ncbi.nlm.nih.gov/pubmed/28257739 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajodo.2016.08.027 |
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