• "Isolated" Amelogenesis Imperfecta Associated with <em>DLX3</em> Mutation: A Clinical Case
• 17q21.32-q22 Deletion in a girl with osteogenesis imperfecta, tricho-dento-osseous syndrome, and intellectual disability
• A 4 bp deletion mutation in DLX3 enhances osteoblastic differentiation and bone formation in vitro
• A clinical case of tricho-dento-osseous syndrome
• A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families
• A de novo germline mutation of DLX3 in a Brown Swiss calf with tricho-dento-osseus-like syndrome
• A dominant mutation etiologic for human tricho-dento-osseous syndrome impairs the ability of DLX3 to downregulate deltaNp63alpha
• A dominant mutation etiologic for human tricho-dento-osseous syndrome impairs the ability of DLX3 to downregulate ΔNp63α
• A novel DLX3 mutation causes tricho-dento-osseous syndrome with abnormal enamel structure and formation
• A patient with melorheostosis manifesting with features similar to tricho-dento-osseous syndrome: a case report
• Amelogenesis imperfecta with taurodontism
• Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: separate conditions or a spectrum of disease?
• An unusual case of tricho-dento-osseous syndrome
• Analysis of the tricho-dento-osseous syndrome genotype and phenotype
• Characterization and mRNA expression in an unusual odontogenic lesion in a patient with tricho-dento-osseous syndrome
• Clinical aspects of dental anomalies
• Clinical features of tricho-dento-osseous syndrome and presentation of three new cases: an addition to clinical heterogeneity
• Clinical heterogeneity in the tricho-dento-osseous syndrome
• Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level
• Comparative study of MSX-2, DLX-5, and DLX-7 gene expression during early human tooth development
• Craniofacial morphology of the tricho-dento-osseous syndrome
• Craniofacial syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis
• Craniofacial variations in the tricho-dento-osseous syndrome
• Dental abnormalities in the tricho-dento-osseous syndrome
• Dental management of tricho-dento-osseous syndrome in adolescent patients: Literature review and case presentation
• DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome
• DLX3 epigenetically regulates odontoblastic differentiation of hDPCs through H19/miR-675 axis
• DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes
• DLX3 interacts with GCM1 and inhibits its transactivation-stimulating activity in a homeodomain-dependent manner in human trophoblast-derived cells
• Dlx3 is a crucial regulator of hair follicle differentiation and cycling
• DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism
• DLX3 mutation in a new family and its phenotypic variations
• DLX3 mutation negatively regulates odontogenic differentiation of human dental pulp cells
• DLX3 negatively regulates osteoclastic differentiation through microRNA-124
• DLX3 promotes bone marrow mesenchymal stem cell proliferation through H19/miR-675 axis
• DLX3-Dependent Regulation of Ion Transporters and Carbonic Anhydrases is Crucial for Enamel Mineralization
• Enamel structure and composition in the tricho-dento-osseous syndrome
• Expression pattern of Dlx3 during cell differentiation in mineralized tissues
• Genetic linkage of the tricho-dento-osseous syndrome to chromosome 17q21
• Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
• In vivo impact of a 4 bp deletion mutation in the DLX3 gene on bone development
• Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome
• Interradicular dentin dysplasia associated with amelogenesis imperfecta with taurodontism or trichodentoosseous syndrome: a diagnostic dilemma
• miR-675 promotes odontogenic differentiation of human dental pulp cells by epigenetic regulation of DLX3
• Molecular consequences of a frameshifted DLX3 mutant leading to Tricho-Dento-Osseous syndrome
• Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family
• Mutant <em>dlx3b</em> disturbs normal tooth mineralization and bone formation in zebrafish
• Mutant DLX 3 disrupts odontoblast polarization and dentin formation
• Non-syndromic generalised hypotaurodontism in a case of Stage III Grade C periodontitis
• Novel DLX3 variant identified in a family with tricho-dento-osseous syndrome
• Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho-dento-osseous syndrome
• Osteogenesis imperfecta, tricho-dento-osseous syndrome and intellectual disability: a familial case with 17q21.33-q22 (COL1A1 and DLX3) deletion and 7q32.3-q33 duplication resulting from a reciprocal interchromosomal insertion
• Periodontal management and restoration of an amelogenesis imperfecta patient: a case report
• Salt Dependence of DNA Binding Activity of Human Transcription Factor Dlx3
• Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome
• Severely hypoplastic amelogenesis imperfecta with taurodontism
• Structural hair shaft abnormalities in hypomelanosis of ito and other ectodermal dysplasias
• Systemic disorders and their influence on the development of dental hard tissues: a literature review
• Taurodontism of the mandibular first permanent molar distinguishes between the tricho-dento-osseous (TDO) syndrome and amelogenesis imperfecta
• The tricho-dento-osseous (TDO) syndrome
• Transcriptional factor DLX3 promotes the gene expression of enamel matrix proteins during amelogenesis
• Tricho-dento-osseous syndrome
• Tricho-dento-osseous syndrome
• Tricho-dento-osseous syndrome
• Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions
• Tricho-dento-osseous syndrome and precocious eruption
• Tricho-dento-osseous syndrome: a scanning electron microscopic analysis
• Tricho-dento-osseous syndrome: diagnosis and dental management
• Tricho-dento-osseous syndrome: heterogeneity or clinical variability
• Tricho-dento-osseous syndrome. Features of the hair and teeth
• Uncombable hair and atopic dermatitis in a case of trichodento-osseous syndrome
• Woolly hair in tricho-dento-osseous syndrome