Mutational analysis of X-linked amelogenesis imperfecta in multiple families
Author:
Publisher
Elsevier BV
Subject
Cell Biology,General Dentistry,General Medicine,Otorhinolaryngology
Reference22 articles.
1. Amelogenesis imperfecta-towards a new classification;Aldred;Oral Dis.,1995
2. Genetic heterogeneity in X-linked amelogenesis imperfecta;Aldred;Genomics,1992
3. Identification of a nonsense mutation the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1);Aldred;Hum. Genet.,1992
4. Scanning electron microscopic studies of deciduous teeth in X-linked amelogenesis imperfecta;Aldred;Journal Oral Pathology Medicine,1992
5. An amelogenin gene defect associated with human x-linked amelogenesis imperfecta;Collier;Archs. Oral Biol.,1997
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1. AMELX Mutations and Genotype–Phenotype Correlation in X-Linked Amelogenesis Imperfecta;International Journal of Molecular Sciences;2024-06-01
2. An Intron c.103-3T>C Variant of the AMELX Gene Causes Combined Hypomineralized and Hypoplastic Type of Amelogenesis Imperfecta: Case Series and Review of the Literature;Genes;2022-07-18
3. A Novel AMELX Mutation, Its Phenotypic Features, and Skewed X Inactivation;Journal of Dental Research;2019-06-11
4. Dose-Dependent Rescue of KO Amelogenin Enamel by Transgenes in Vivo;Frontiers in Physiology;2017-11-16
5. Deletion of Slc26a1 and Slc26a7 Delays Enamel Mineralization in Mice;Frontiers in Physiology;2017-05-16
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