Associated Papers
Novel MSX1 Gene Variants in Chinese Children with Non-Syndromic Tooth Agenesis: A Clinical and Genetic Analysis.
Ding T et al.
Children (basel, Switzerland), 2024
39767847 (PubMed )
Supplement: children-11-01418-s001.zip › Supplement_Table_S1.xlsx › Sheet1
Orodental malformations associated with human MSX1 sequence variants.
Wang YL et al.
Journal of the American Dental Association (1939), 2024
Characterization of novel MSX1 variants causally associated with non-syndromic oligodontia in Chinese families.
Zhao Y et al.
Molecular Genetics & Genomic Medicine, 2024
38069551 (PubMed )
Supplement: MGG3-12-e2334-s002.xls › Sheet1
Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes : Analysis of a Turkish cohort.
Keskin G et al.
Journal of Orofacial Orthopedics = Fortschritte Der Kieferorthopadie : Organ/official Journal Deutsche Gesellschaft Fur Kieferorthopadie, 2022
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