Disease: Tricho-dento-osseous syndrome 1
- 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
- Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: separate conditions or a spectrum of disease?
- Clinical features of tricho-dento-osseous syndrome and presentation of three new cases: an addition to clinical heterogeneity
- 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
- Craniofacial syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis
- 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 mutation in a new family and its phenotypic variations
- DLX3 mutation negatively regulates odontogenic differentiation of human dental pulp cells
- Expression pattern of Dlx3 during cell differentiation in mineralized tissues
- 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
- 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
- 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
- Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions
- Tricho-dento-osseous syndrome: a scanning electron microscopic analysis
- Tricho-dento-osseous syndrome. Features of the hair and teeth
