Associated Papers
Genotypic and phenotypic correlations in tooth agenesis: insights from WNT10A and EDA mutations in syndromic and non-syndromic forms.
Wu Y et al.
Human Genetics, 2024
Orodental malformations associated with human MSX1 sequence variants.
Wang YL et al.
Journal of the American Dental Association (1939), 2024
MSX1 involved selective tooth agenesis and abnormal labial frenum, pedigree, and retrospective study.
Zhu Y et al.
Oral Diseases, 2023
Two novel mutations in MSX1 causing oligodontia.
Yang L et al.
Plos One, 2020
31914153 (PubMed )
Supplement: pone.0227287.s007.docx
Simultaneous Occurence of an Autosomal Dominant Inherited MSX1 Mutation and an X-linked Recessive Inherited EDA Mutation in One Chinese Family with Non-syndromic Oligodontia.
Zhang XX et al.
The Chinese Journal of Dental Research, 2015
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