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Molecular Basis for Craniofacial Phenotypes Caused by Sclerostin Deletion
Some genetic disorders are associated with distinctive facial features, which can aid in diagnosis. While considerable advances have been made in identifying causal genes, relatively little progress has been made toward understanding how a particular genotype results in a characteristic craniofacial...
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| Publicado no: | J Dent Res |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7903846/ https://ncbi.nlm.nih.gov/pubmed/33078679 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034520963584 |
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