Utilising Next‐Generation Sequencing to Explore the Molecular Etiology of Short Root Anomaly
Our data demonstrates that a mutation in the H1C gene may have a causal role in AD SRA.
Authors
- David K. Crossman (ORCID: https://orcid.org/0000-0002-0981-169X)
- Quamarul Hassan (ORCID: https://orcid.org/0000-0002-4690-473X)
- Ejvis Lamani (ORCID: https://orcid.org/0000-0001-6341-3134)
- Mary MacDougall (ORCID: https://orcid.org/0000-0002-0993-864X)
- Emily A. Joy
Institutions
- University of British Columbia (CA)
- University of Alabama at Birmingham (US)
Publication Details
- Journal
- Orthodontics and Craniofacial Research
- Published
- 2025-08-09
- DOI
- https://doi.org/10.1111/ocr.70015
- Primary Topic
- dental development and anomalies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- American Association of Orthodontists Foundation
- National Institute of Dental and Craniofacial Research
- National Center for Advancing Translational Sciences