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Healthcare (Basel, Switzerland)|September 28, 2021
From Child to Adulthood, a Multidisciplinary Approach of Multiple Microdontia Associated with Hypodontia: Case Report Relating a 15 Year-Long Management and Follow-UpCharlotte Thomas, Frédéric Vaysse, Teva Courset, et al.
Quintessence International (Berlin, Germany : 1985)|October 21, 2022
Oral health status in patients with inherited epidermolysis bullosa: a comparative multicenter studyClara Joseph, Mathieu Marty, Sophie-Myriam Dridi, et al.
Pediatric Research|August 31, 2006
High proportion of pituitary abnormalities and other congenital defects in children with congenital nasal pyriform aperture stenosisSophie Guilmin-Crépon, Catherine Garel, Clarisse Baumann, et al.
European Journal of Dentistry|January 7, 2021
Morbidity and Mortality Review in a University Dental Hospital: A Necessary Tool to Improve Quality of CareRémi Esclassan, Marie-Cécile Valera, Jean Marc Bergia, et al.
Frontiers in Physiology|June 30, 2017
Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified <i>MMP20</i> Mutations Causing Amelogenesis ImperfectaBarbara Gasse, Megana Prasad, Sidney Delgado, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasiaJulie Plaisancié, Isabelle Bailleul-Forestier, Véronique Gaston, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 5, 2022
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defectsAuriane Cospain, Ana Rivera-Barahona, Erwan Dumontet, et al.
Human Molecular Genetics|February 12, 2015
Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfectaMathilde Huckert, Corinne Stoetzel, Supawich Morkmued, 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.
Nucleic Acids Research|November 13, 2013
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype dataSebastian Köhler, Sandra C Doelken, Christopher J Mungall, et al.
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