What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndr...
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
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Berlin/Heidelberg: Springer Berlin Heidelberg
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English
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Berlin/Heidelberg: Springer Berlin Heidelberg
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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 due to population-specific SNP variants. Therefore, we...
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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
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TN_cdi_doaj_primary_oai_doaj_org_article_ec7031a8342549959a11cca4ad3e0dbe
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_ec7031a8342549959a11cca4ad3e0dbe
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ISSN
2196-1042,1723-7785
E-ISSN
2196-1042
DOI
10.1186/s40510-024-00532-4