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
MSX1 involved selective tooth agenesis and abnormal labial frenum, pedigree, and retrospective study.
Zhu Y et al.
Oral Diseases, 2023
MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.
Liang J et al.
European Journal of Human Genetics : Ejhg, 2016
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