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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Bibliographic Details
Published in:	J Dent Res
Main Authors:	Chen, J., Yuan, X., Pilawski, I., Liu, X., Delgado-Calle, J., Bellido, T., Turkkahraman, H., Helms, J.A.
Format:	Artigo
Language:	Inglês
Published:	SAGE Publications 2020
Subjects:	Research Reports
Online Access:	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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Molecular Basis for Craniofacial Phenotypes Caused by Sclerostin Deletion

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