• A case of multiple rootless teeth: A case report and review
• A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene
• A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family
• A novel mutation in the DSPP gene associated with dentinogenesis imperfecta type II
• A rare case diagnosed as dentin dysplasia type II
• A scanning electron microscopic study of dentin dysplasia type II in primary dentition
• A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement
• An unusual variation of radicular dentin dysplasia: A rare case report with review of literature
• Astacin proteases cleave dentin sialophosphoprotein (Dspp) to generate dentin phosphoprotein (Dpp)
• Clinical approach to rhizomicry based on a case of dentine dysplasia type 1
• Cone-beam CT imaging characteristics of type Ⅰ dentin dysplasia during the dental replacement period
• CONTRIBUTION TO THE PROSTHETIC SUBSTITUTION OF ROOTLESS TEETH
• Dental characteristics of patients with four different types of skeletal dysplasias
• Dental structural diseases mapping to human chromosome 4q21
• Dentin dysplasia type 1 - clinical management dilemmas: A case report of first-generation sufferers
• Dentin dysplasia Type 1. Root dysplasia
• Dentin dysplasia type I
• Dentin dysplasia type I
• Dentin dysplasia type I - A rare entity
• Dentin dysplasia type I--a case report
• Dentin dysplasia type I-A dental disease with genetic heterogeneity
• Dentin dysplasia type I-novel findings in deciduous and permanent teeth
• Dentin dysplasia type I: a case report and review of the literature
• Dentin dysplasia type I: a scanning electron microscopic analysis of the primary dentition
• Dentin dysplasia type I: report of atypical cases in the permanent and mixed dentitions
• Dentin dysplasia, type II linkage to chromosome 4q
• Dentin dysplasia, type II: report of 2 new families and review of the literature
• Dentin dysplasia: review of the literature and a proposed subclassification based on radiographic findings
• Dentin dysplasia: single-tooth involvement?
• Dentin Sialophophoprotein (DSPP) and Dentin
• Dentinal dysplasia type 1: A 3D micro-computed tomographic study of enamel, dentine and root canal morphology
• Dentinal dysplasia type I: report of a case
• Dentinal dysplasia, type I: report of a case
• Dentinogenesis imperfecta type 2: a case report
• Dentinogenesis imperfecta type II in Swedish children and adolescents
• Diagnostic challenge. Dentin dysplasia, type II
• Disorders of human dentin
• Distinctive role of ACVR1 in dentin formation: requirement for dentin thickness in molars and prevention of osteodentin formation in incisors of mice
• Distribution and structure of dental enamel in incisors of Tabby mice
• DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes
• Endodontic therapy on a dentition exhibiting multiple periapical radiolucencies associated with dentinal dysplasia Type 1
• Guided endodontic treatment of multiple teeth with dentin dysplasia: a case report
• Hereditary dentin defects
• Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia
• Hereditary pathology of the enamel and dentin. A review of molecular genetic research
• Hereditary pattern for dentinal dysplasia type Id: a case report
• Histological and Ultrastructure Analysis of Dentin Dysplasia Type I in Primary Teeth: A Case Report
• Human genes for dental anomalies
• Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan family
• Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification
• MEPE/OF45, a new dentin/bone matrix protein and candidate gene for dentin diseases mapping to chromosome 4q21
• Mouse Dspp frameshift model of human dentinogenesis imperfecta
• Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I
• Mutation of dentin sialophosphoprotein and hereditary malformations of dentin
• Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in <em>COL1A2</em>
• PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and Microcephaly
• Porcine dentin sialoprotein glycosylation and glycosaminoglycan attachments
• Prevalence of dental anomalies among 7- to 35-year-old people in Hamadan, Iran in 2012-2013 as observed using panoramic radiographs
• Radicular (type 1) dentin dysplasia
• Reduced expression of dentin sialophosphoprotein is associated with dysplastic dentin in mice overexpressing transforming growth factor-beta 1 in teeth
• Refined mapping of the human dentin sialophosphoprotein (DSPP) gene within the critical dentinogenesis imperfecta type II and dentin dysplasia type II loci
• Restorative treatment in a case of amelogenesis imperfecta and 9-year follow-up: a case report
• Revision of the 1992 edition of the WHO histological typing of odontogenic tumors. A suggestion
• Reviving a Smile: A Multidisciplinary Approach to Dentin Dysplasia
• Rootless teeth and Condylar osteolysis
• Rough hypoplastic amelogenesis imperfecta with follicular hyperplasia
• Spatial expression of Cbfa1/Runx2 isoforms in teeth and characterization of binding sites in the DSPP gene
• Spectrum of dentin dysplasia in a family: case report and literature review
• Symmetric multiquadrant isolated dentin dysplasia (SMIDD), a unique presentation mimicking dentin dysplasia type 1b
• The dentin phosphoprotein repeat region and inherited defects of dentin
• The diagnosis of dentinal dysplasia Type 1
• The diagnosis of dentinal dysplasia Type I
• The First Compound Heterozygous Mutations of DMP1 Causing Rare Autosomal Recessive Hypophosphatemic Rickets Type 1
• The Modified Shields Classification and 12 Families with Defined <em>DSPP</em> Mutations
• Type I dentin dysplasia: report of two cases
• Type I Dentin Dysplasia: The Literature Review and Case Report of a Family Affected by Misrecognition and Late Diagnosis
• Type-1 Dentine Dysplasia – Diagnostic and Clinical Challenges in Restorative Management
• Ultrastructure of dentin matrix in heritable dentin defects
• Unequal Impact of <em>COL1A1</em> and <em>COL1A2</em> Variants on Dentinogenesis Imperfecta
• Vacuolar protein sorting 4B regulates the proliferation and odontoblastic differentiation of human dental pulp stem cells through the Wnt-β-catenin signalling pathway
• Variation of dentin dysplasia type I: report of atypical findings in the permanent dentition
• VPS4B deficiency causes early embryonic lethality and induces signal transduction disorders of cell endocytosis
• Vps4b heterozygous mice do not develop tooth defects that replicate human dentin dysplasia I
• VPS4B mutation impairs the osteogenic differentiation of dental follicle cells derived from a patient with dentin dysplasia type I