A novel pathogenic mutation in TSPEAR associated with sensorineural hearing loss: a case report and review of the literature. [PDF]
Ahmadkhani A +5 more
europepmc +1 more source
Dental Manifestations in Children Affected by Hypophosphatemic Rickets: A Systematic Review and Meta-Analysis. [PDF]
Allam A +4 more
europepmc +1 more source
Full-Mouth Reconstruction in Amelogenesis Imperfecta: A Case Report. [PDF]
Marghalani AA.
europepmc +1 more source
Craniofacial Radiographic Features in Amelogenesis Imperfecta: A Case-Control Study. [PDF]
Chadli K +3 more
europepmc +1 more source
Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies. [PDF]
Ruangchan C +15 more
europepmc +1 more source
Silver-Russell syndrome: phenotype features and oral health status. [PDF]
Piekoszewska-Ziętek P +4 more
europepmc +1 more source
Abnormal dental phenotypes in GAPO syndrome: A descriptive study with a new ANTXR1 variant & insights on teeth eruption. [PDF]
El-Moataz Bellah Ahmed N +3 more
europepmc +1 more source
Orthodontic management of amelogenesis imperfecta: A case report. [PDF]
Jha K, Adhikari M, Shrestha S, Pandey A.
europepmc +1 more source
Genotype-phenotype analysis and functional study of three novel <i>LRP6</i> variants in non-syndromic oligodontia. [PDF]
Yuan Y +12 more
europepmc +1 more source
Dental Anomalies in Saudi Arabia: A Systematic Review. [PDF]
Aljohani K +3 more
europepmc +1 more source

