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Journal Article
JOURNAL OF CLINICAL PEDIATRIC DENTISTRY, ISSN 1053-4628, 2019, Volume 43, Issue 3, pp. 147 - 154
Dentinogenesis Imperfecta type II (DI2), also known as hereditary opalescent dentin, is one of the most common genetic disorders affecting the structure of... 
Dentinogenesis Imperfecta Type II | Scoping Review | DENTISTRY, ORAL SURGERY & MEDICINE | MUTATION | DENTIN DEFECTS | REHABILITATION | FRACTURES | PEDIATRICS | PATIENT | Management | Children | MANIFESTATIONS | Dentin | Pediatrics | Genetic counseling | Enamel | Teeth | Classification | Systematic review | Dentistry | Mutation
Journal Article
Journal Article
Fetal and Pediatric Pathology, ISSN 1551-3815, 05/2019, Volume 38, Issue 3, pp. 263 - 271
Background: Osteogenesis imperfect (OI) type II is a genetic disorder of bone characterized by bone fragility, multiple fractures, severe bowing and shortening... 
balanced translocation | osteogenesis imperfecta type II | COLI 1 and COLI 2 genes | fetal autopsy
Journal Article
Journal Article
European Journal of Paediatric Dentistry, ISSN 1591-996X, 2018, Volume 19, Issue 4, pp. 303 - 306
Dentinogenesis imperfecta (DI) is an autosomal dominant genetic disease that affects both deciduous and permanent teeth, with an incidence of 1 out of 6,000 to... 
Dentinogenesis imperfecta | Adhesive restorative rehabilitation
Journal Article
Gynecologic and Obstetric Investigation, ISSN 0378-7346, 03/2015, Volume 79, Issue 2, pp. 101 - 104
Aim: To analyze COL1A1/2 mutations in prenatal-onset OI for determine the proportion of mutations in type I collagen genes among prenatal onset OI and to... 
COL1A1 gene | COL1A2 gene | Mutation | Fetal osteogenesis imperfecta | Gene sequencing
Journal Article
Human Genetics, ISSN 0340-6717, 2/2005, Volume 116, Issue 3, pp. 186 - 191
The current system for the classification of hereditary defects of tooth dentin is based upon clinical and radiographic findings and consists of two types of... 
LifeSciences | 6-GENERATION FAMILY | DENTIN | GENETICS & HEREDITY | Protein Precursors - genetics | Humans | Child, Preschool | Infant | Male | Genetic Variation | Sialoglycoproteins | Extracellular Matrix Proteins | Pedigree | Phosphoproteins | Dentinogenesis Imperfecta - classification | Female | Mutation | Dentinogenesis Imperfecta - genetics
Journal Article
Pan African Medical Journal, ISSN 1937-8688, 05/2015, Volume 21, p. 11
We report a new case of osteogenesis imperfecta (OI) type II which is a perinatal lethal form. First trimester ultrasound didn't identified abnormalities.... 
Osteogenesis imperfecta | Newborn | Prenatal diagnosis | Pregnancy | Osteogenesis Imperfecta - diagnosis | Humans | Fatal Outcome | Osteogenesis Imperfecta - physiopathology | Respiratory Insufficiency - etiology | Adult | Female | Ultrasonography, Prenatal - methods | Infant, Newborn
Journal Article
Folia Histochemica et Cytobiologica, ISSN 0239-8508, 2013, Volume 51, Issue 3, pp. 244 - 247
The morphological abnormalities of the teeth of patients affected by dentinogenesis imperfecta type 2 (DI-II) may underlie the difficulties with the clinical... 
Dentin | Tooth structure | Dentinogenesis imperfecta | SEM | Enamel | dentinogenesis imperfecta | tooth structure | BIOCHEMISTRY & MOLECULAR BIOLOGY | enamel | DISORDERS | dentin | CELL BIOLOGY | Young Adult | Dental Enamel - ultrastructure | Dentin - ultrastructure | Humans | Dentinogenesis Imperfecta - pathology | Molar - ultrastructure
Journal Article