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Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis
Tooth agenesis is a common craniofacial abnormality in humans and represents failure to develop 1 or more permanent teeth. Tooth agenesis is complex, and variations in about a dozen genes have been reported as contributing to the etiology. Here, we combined whole-exome sequencing, array-based genoty...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Dent Res |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
SAGE Publications
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6728545/ https://ncbi.nlm.nih.gov/pubmed/28813618 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034517724149 |
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