Associated Papers
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
Mutations in WNT10A are present in more than half of isolated hypodontia cases.
van den Boogaard MJ et al.
Journal of Medical Genetics, 2012
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