Associated Papers
Current insights on the genetics and mechanisms of MSX1-associated cleft palate.
Myo AC et al.
Frontiers in Dental Medicine, 2025
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
EDA Variants Are Responsible for Approximately 90% of Deciduous Tooth Agenesis.
Su L et al.
International Journal of Molecular Sciences, 2024
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
MSX1 involved selective tooth agenesis and abnormal labial frenum, pedigree, and retrospective study.
Zhu Y et al.
Oral Diseases, 2023
Novel MSX1 variants identified in families with nonsyndromic oligodontia.
Zheng J et al.
International Journal of Oral Science, 2021
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