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
Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia.
Bonczek O et al.
Plos One, 2018
Non-syndromic severe hypodontia caused by a novel frameshift insertion mutation in the homeobox of the MSX1 gene.
Abid MF et al.
Archives of Oral Biology, 2017
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