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
Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia.
Bonczek O et al.
Plos One, 2018
A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesis.
AlFawaz S et al.
Archives of Oral Biology, 2015
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