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

• Main Authors: Nora Alhazmi (Author), Ali Alaqla (Author), Bader Almuzzaini (Author), Mohammed Aldrees (Author), Ghaida Alnaqa (Author), Farah Almasoud (Author), Omar Aldibasi (Author), Hala Alshamlan (Author)
• Format: Book
• Published: SpringerOpen, 2024-08-01T00:00:00Z.
• Subjects: article
• Online Access: 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...