DLX3 Homeodomain Mutations Cause Tricho-Dento-Osseous Syndrome with Novel Phenotypes

Craniofacial morphology of the tricho-dento-osseous syndrome

(2010) Katherine Kula et al.   CLINICAL GENETICS

Taurodontism of the mandibular first permanent molar distinguishes between the tricho-dento-osseous (TDO) syndrome and amelogenesis imperfecta

(2010) W. Kim Seow   CLINICAL GENETICS

Mutant DLX 3 disrupts odontoblast polarization and dentin formation

(2010) S.J. Choi et al.   DEVELOPMENTAL BIOLOGY

Unkämmbare Haare und atopische Dermatitis bei tricho-dentoossärem Syndrom

(2010) Dagmara E. Y. Mayer et al.   JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT

DLX3 Mutation in a New Family and Its Phenotypic Variations

(2009) S.-K. Lee et al.   JOURNAL OF DENTAL RESEARCH

DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome

(2008) J. Timothy Wright et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Dlx3 is a crucial regulator of hair follicle differentiation and cycling

(2008) J. Hwang et al.   DEVELOPMENT

In vivo impact of a 4 bp deletion mutation in the DLX3 gene on bone development

(2008) S.J. Choi et al.   DEVELOPMENTAL BIOLOGY

Molecular Consequences of a Frameshifted DLX3 Mutant Leading to Tricho-Dento-Osseous Syndrome

(2008) Olivier Duverger et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

A 4 bp deletion mutation in DLX3 enhances osteoblastic differentiation and bone formation in vitro

(2007) Sun Jin Choi et al.   BONE