Associated Papers
Screening for MSX1 and PAX9 gene variants among hypodontia patients in the Jordanian population.
Quran A et al.
Cellular and Molecular Biology (noisy-le-grand, France), 2026
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
MSX1 involved selective tooth agenesis and abnormal labial frenum, pedigree, and retrospective study.
Zhu Y et al.
Oral Diseases, 2023
Two novel mutations in MSX1 causing oligodontia.
Yang L et al.
Plos One, 2020
31914153 (PubMed )
Supplement: pone.0227287.s007.docx
Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia.
Bonczek O et al.
Plos One, 2018
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