What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndromic hypodontia? A case-control study in orthodontically treated patients

• Autores principales: Nora Alhazmi (Autor), Ali Alaqla (Autor), Bader Almuzzaini (Autor), Mohammed Aldrees (Autor), Ghaida Alnaqa (Autor), Farah Almasoud (Autor), Omar Aldibasi (Autor), Hala Alshamlan (Autor)
• Formato: Libro
• Publicado: SpringerOpen, 2024-08-01T00:00:00Z.
• Materias: article
• Acceso en línea: Connect to this object online.

Abstract Background Hypodontia is the most prevalent dental anomaly in humans, and is primarily attributed to genetic factors. Although genome-wide association studies (GWAS) have identified single-nucleotide polymorphisms (SNP) associated with hypodontia, genetic risk assessment remains challenging...