All children, who were born in 2004 and had undergone surgical treatment for recurrent acute tonsillitis and/or acute otitis media at the ear, nose and throat clinic (ENT) between 2004 and 2010, were called on dental examination and blood sampling. Out of 441 invitees, 113 children and their parents/legal guardians agreed to participate. The following data from this group of subjects are presented: the presence of clinical signs of molar–incisor hypomineralisation (MIH), the distribution of human leukocyte antigen (HLA) alleles DQ2 and DQ8 and eight single nucleotide polymorphisms (SNPs) located in amelogenesis-related genes (rs3796704 in the ENAM gene, rs546778141 in the AMBN gene, rs2106416 in the AMELX gene, rs7660807 and rs35286445 in t...
Background: Early childhood caries (ECC) is one of the most common diseases of childhood. The etiolo...
Identification of an Enamelin Defect Resulting in Amelogenesis ImperfectaJessica Claire MassieABSTRA...
Objectives: This study aimed to comprehensively characterise genetic variants of amelogenesis imperf...
Objective: The present study searched for evidence of possible associations between some genetic fac...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Despite some evidence of genetic and en...
OBJECTIVES: This genome-wide association study (GWAS) investigated the relationship between molar-in...
Amelogenesis imperfecta (AI) represents hereditary conditions affecting the quality and quantity of ...
Skulskaya S. V., Verbitskaya T. G., Denga O. V. PROBABILITY OF DENTAL PATHOLOGY DEVELOPMENT IN CHILD...
Indiana University-Purdue University Indianapolis (IUPUI)Purpose of the Study: Determine if there i...
Molar incisor hypomineralization (MIH) is an enamel condition characterized by lesions ranging in co...
Amelogenesis imperfecta (AI) represents hereditary conditions affecting the quality and quantity of ...
Five mutations in the ENAM gene have been found to cause hypoplastic amelogenesis imperfecta (AI), w...
Determining genotype–phenotype correlations in patients with hypodontia is important for understandi...
Determining genotype–phenotype correlations in patients with hypodontia is important for understandi...
Amelogenesis imperfecta is a group of inherited diseases affecting the quality and quantity of denta...
Background: Early childhood caries (ECC) is one of the most common diseases of childhood. The etiolo...
Identification of an Enamelin Defect Resulting in Amelogenesis ImperfectaJessica Claire MassieABSTRA...
Objectives: This study aimed to comprehensively characterise genetic variants of amelogenesis imperf...
Objective: The present study searched for evidence of possible associations between some genetic fac...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Despite some evidence of genetic and en...
OBJECTIVES: This genome-wide association study (GWAS) investigated the relationship between molar-in...
Amelogenesis imperfecta (AI) represents hereditary conditions affecting the quality and quantity of ...
Skulskaya S. V., Verbitskaya T. G., Denga O. V. PROBABILITY OF DENTAL PATHOLOGY DEVELOPMENT IN CHILD...
Indiana University-Purdue University Indianapolis (IUPUI)Purpose of the Study: Determine if there i...
Molar incisor hypomineralization (MIH) is an enamel condition characterized by lesions ranging in co...
Amelogenesis imperfecta (AI) represents hereditary conditions affecting the quality and quantity of ...
Five mutations in the ENAM gene have been found to cause hypoplastic amelogenesis imperfecta (AI), w...
Determining genotype–phenotype correlations in patients with hypodontia is important for understandi...
Determining genotype–phenotype correlations in patients with hypodontia is important for understandi...
Amelogenesis imperfecta is a group of inherited diseases affecting the quality and quantity of denta...
Background: Early childhood caries (ECC) is one of the most common diseases of childhood. The etiolo...
Identification of an Enamelin Defect Resulting in Amelogenesis ImperfectaJessica Claire MassieABSTRA...
Objectives: This study aimed to comprehensively characterise genetic variants of amelogenesis imperf...