Caleidox: DENTINOGENESIS IMPERFECTA

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Artículos y Publicaciones acerca de DENTINOGENESIS IMPERFECTA que son de acceso gratuito:

• Prevalence and distribution of selected developmental dental anomalies in an Indian population. (2011)

• A novel DSPP mutation causes dentinogenesis imperfectatype II in a large Mongolian family (2010)

• A Novel Mutationin the DSPP Gene Associated with Dentinogenesis Imperfecta Type II (2009) 

• Dentinogenesis imperfecta: a case report. (2008)

• The role of dentists in diagnosing osteogenesis imperfecta in patients with dentinogenesis imperfecta (2008)

• Dentinogenesis imperfecta: a review and case report of a family over four generations.(2008)

• Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta. (2008)

• Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia. (2008)

• Phenotype characterization and DSPP mutational analysis of three Brazilian dentinogenesis imperfecta type II families (2008)

• Dentinogenesis imperfecta type II. an affect family saga (2007)

• Osteogénesis imperfecta: caso clínico y actualización (2007)

• Osteogénesis  imperfecta. Revisón Bibliográfica (2007)

• A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family. (2007)

• Dentinogénesis imperfecta: Reporte de un caso (2006)

• Esthetic Reconstruction of Teeth in Patient with Dentinogenesis Imperfecta – A Case Report (2006) 

• Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21.(2006)

• Mutational hot spot in the DSPP gene causingdentinogenesis imperfecta type II (2005)

• Dentinogenesis Imperfecta Associated with Osteogenesis Imperfecta: Report of Two Cases (2003)

• Orthodontic and orthognathic management of a patient with osteogenesis imperfecta and dentinogenesis imperfecta: a case report (2003)

• Dentinogenesis imperfecta associated with osteogenesis imperfecta: report of two cases. (2003)

• Síndrome de escleras azules (2002)

• Dentinogenesis imperfecta: an early treatmentstrategy (2001)

• Intrafibrillar mineral may be absent in dentinogenesis imperfecta type II (2001) 

• The Non-collagenous Dentin Matrix Proteins are Involved in Dentinogenesis Imperfecta Type II (2000)

• Genetic Linkage of the Dentinogenesis Imperfecta Type III Locus to Chromosome 4q (1999)

• Familial tarda type osteogenesis imperfecta with dentinogenesisimperfecta Type I. Case report (1997)

• Immunoreactivityof Tenascin-C in Dentin Matrix in Dentinogenesis Imperfecta Associated withosteogenesis imperfecta (1996)

• Genetic Mapping of the Dentinogenesis Imperfecta Type II Locus (1995)

• Dentin Phosphoprotein Gene Locus Is Not Associated with Dentinogenesis Imperfecta Types II and III (1992) 

• Dentinogénesis imperfecta. Presentación de un caso clínico (1984)

• The Inorganic Phase in Dentinogenesis imperfecta (1981)

• Familial dentinogenesis imperfecta, blue sclerae, and wormian bones without fractures: another type of osteogenesis imperfecta? (1981)

• Dentinogenesis Imperfecta: Genetic Variations in a Six-Generation Family (1969)