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2. PAX9 mutations and genetic synergism in familial tooth agenesis

6. Dental malformations associated with biallelic MMP20 mutations

7. ENAM mutations and digenic inheritance

9. AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout‐NLS‐lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue‐specificity

11. Mutations in RELT cause autosomal recessive amelogenesis imperfecta

15. Fam83h null mice support a neomorphic mechanism for human ADHCAI

16. The dentin phosphoprotein repeat region and inherited defects of dentin

18. Taurodontism, variations in tooth number, and misshapened crowns inWnt10anull mice and human kindreds

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