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Acta Biomaterialia|August 13, 2023
Multi-scale characterization of Developmental Defects of Enamel and their clinical significance for diagnosis and treatmentSophia Houari, Karen DeRocher, Tran Thu Thuy, et al.BMC Musculoskeletal Disorders|August 23, 2020
Cherubism as a systemic skeletal disease: evidence from an aggressive caseAnne Morice, Aline Joly, Manon Ricquebourg, et al.Oral Diseases|November 21, 2024
Dental and Craniofacial Anomalies in Fanconi Anemia: A Systematic Review and Additional 46 ReportsPaula Alves da Silva Rocha, Nayara Conceição Marcos Santana, José Alcides Almeida de Arruda, et al.Scientific Reports|April 25, 2024
Gingival proteomics reveals the role of TGF beta and YAP/TAZ signaling in Raine syndrome fibrosisCláudio Rodrigues Rezende Costa, Rym Chalgoumi, Amina Baker, et al.The Journal of Craniofacial Surgery|September 4, 2025
Timeline of Amelogenesis Imperfecta ManagementAlexandra Jimenez-Armijo, Paola L Carvajal Monroy, Saranda Ombashi, et al.Journal of Medical Genetics|August 18, 2016
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutationsPaulo Marcio Yamaguti, Francisco de Assis Rocha Neves, Dominique Hotton, et al.American Journal of Medical Genetics. Part A|August 31, 2019
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disordersMuriel de La Dure-Molla, Benjamin Philippe Fournier, Maria Cristina Manzanares, et al.Clinical Genetics|June 2, 2025
A Novel Skeletal Dysplasia With Premaxilla Overgrowth, Gingival Hyperplasia, and Dental HypercementosisPaulo Marcio Yamaguti, Shélida Vasconcelos Braz, Audrey Asselin, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 2, 2015
Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel FormationClaire Bardet, Frédéric Courson, Yong Wu, et al.Journal of Medical Genetics|October 28, 2015
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvementMegana K Prasad, Véronique Geoffroy, Serge Vicaire, et al.Pageof 12