Disease: Amelogenesis Imperfecta hypomaturation type
- <em>Amelogenesis imperfecta</em>: Next-generation sequencing sheds light on Witkop's classification
- A clinical, genetic, and ultrastructural study of snow-capped teeth: amelogenesis imperfecta, hypomaturation type
- A Fourth <em>KLK4</em> Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities
- A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family
- Amelogenesis Imperfecta: A Non-Invasive Approach to Improve Esthetics in Young Patients. Report of Two Cases
- Clinical findings and long-term managements of patients with amelogenesis imperfecta
- Critical roles for WDR72 in calcium transport and matrix protein removal during enamel maturation
- Dental malformations associated with biallelic MMP20 mutations
- Distal renal tubular acidosis, autoimmune thyroiditis, enamel hypomaturation, and tooth agenesis caused by homozygosity of a novel double-nucleotide substitution in SLC4A4
- Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant
- Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation
- Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta
- Recessive Mutations in <em>ACP4</em> Cause Amelogenesis Imperfecta
- Target gene analyses of 39 amelogenesis imperfecta kindreds
- Trichodentoosseous syndrome: a case report and review of literature
- Unusual extrinsic staining following microabrasion in a girl with amelogenesis imperfecta
- WDR72 Mutations Associated with Amelogenesis Imperfecta and Acidosis