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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of dental research 2021-03, Vol.100 (3), p.310-317
Hauptverfasser: Chen, J., Yuan, X., Pilawski, I., Liu, X., Delgado-Calle, J., Bellido, T., Turkkahraman, H., Helms, J.A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!