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
MSX1 involved selective tooth agenesis and abnormal labial frenum, pedigree, and retrospective study.
Zhu Y et al.
Oral Diseases, 2023
Integrated exome and RNA sequencing of TFE3-translocation renal cell carcinoma.
Sun G et al.
Nature Communications, 2021
34489456 (PubMed )
Supplement: 41467_2021_25618_MOESM6_ESM.xlsx › Somatic_mutations
Novel MSX1 variants identified in families with nonsyndromic oligodontia.
Zheng J et al.
International Journal of Oral Science, 2021
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