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
MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.
Liang J et al.
European Journal of Human Genetics : Ejhg, 2016
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