Results 141 to 150 of about 7,940 (235)
Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report
Dentinogenesis imperfecta (DI) is a hereditary dentin defect caused by an autosomal dominant mutation in dentin sialophosphoprotein gene. Defective dentin development results in discolored teeth that are prone to wear and fracture.
Najmeh Akhlaghi+2 more
doaj
Case of the Month #171: Osteogenesis Imperfecta of the Temporal Bone [PDF]
Aviv, Richard I.+6 more
core +1 more source
Osteogenesis imperfecta and dentinogenesis imperfecta
Chetna Grover+3 more
openalex +1 more source
Unravelling the Genetic Basis of Dentinogenesis Imperfecta
Dr Maleeha Gilani+1 more
openalex +1 more source
Oral health in prevalent types of Ehlers-Danlos syndromes [PDF]
Ainamo J+47 more
core +2 more sources
Dentinogenesis imperfecta: A review and case report of a family over four generations
Sudhir Bhandari, Karneev Pannu
openalex +1 more source
The role of transforming growth factor beta in tertiary dentinogenesis
Tetiana Haniastuti+2 more
openalex +2 more sources
Manifestasi Klinis, Aspek Genetica Molekuler dan Management Dentinogenesis Imperfekta
Olivia Bratanata+2 more
openalex +1 more source