Associated Papers
Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho-dento-osseous syndrome.
Whitehouse LLE et al.
Oral Diseases, 2019
Tricho-dento-osseous syndrome and precocious eruption.
Jain P et al.
Journal of Clinical and Experimental Dentistry, 2017
Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.
Zhao N et al.
Scientific Reports, 2016
27924851 (PubMed )
Supplement: srep38680-s1.pdf
Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta.
Kim YJ et al.
Oral Diseases, 2016
DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes.
Nieminen P et al.
Cells, Tissues, Organs, 2011
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