Associated Papers
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
Patterns of Dental Agenesis Highlight the Nature of the Causative Mutated Genes.
Fournier BP et al.
Journal of Dental Research, 2018
29879364 (PubMed )
Supplement: ds_10.1177_0022034518777460.pdf
An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese family.
Tatematsu T et al.
Plos One, 2015
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