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R-twist gene expression during rat palatogenesisEvolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis ImperfectaPathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutationsAmelogenesis imperfectaMutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.From the transcription of genes involved in ectodermal dysplasias to the understanding of associated dental anomalies.A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvementDetection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar.A possible cranio-oro-facial phenotype in Cockayne syndrome.RSK2 is a modulator of craniofacial development.Retinoic Acid Excess Impairs Amelogenesis Inducing Enamel Defects.Enamel and dental anomalies in latent-transforming growth factor beta-binding protein 3 mutant mice.Hypophosphatasia: diagnosis and clinical signs - a dental surgeon perspective.Amelogenesis Imperfecta: 1 Family, 2 Phenotypes, and 2 Mutated Genes.Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.Roles of retinoic acid receptors and of Hox genes in the patterning of the teeth and of the jaw skeleton.Effects of retinoids on tooth morphogenesis and cytodifferentiations, in vitro.Involvement of cellular retinoic acid-binding proteins I and II (CRABPI and CRABPII) and of the cellular retinol-binding protein I (CRBPI) in odontogenesis in the mouse.Corrigendum: Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar.Oral health of children with juvenile idiopathic arthritis.Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.SLC13A5 is the second gene associated with Kohlschütter-Tönz syndrome.In vitro effects of retinoic acid on mouse incisor development.Hypophosphatasia: oral cavity and dental disorders.Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.Oro-dental features as useful diagnostic tool in Rubinstein-Taybi syndrome.Oral health of children with intractable epilepsy attending the UK National Centre for Young People with Epilepsy.A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.Gene expression during palate fusion in vivo and in vitro.Expression of p21(WAF1/CIP1) during mouse odontogenesis.Expression of nuclear retinoic acid receptors during mouse odontogenesis.Abstracts of the 6th International Alkaline Phosphatase and Hypophosphatasia Symposium, May 16-19, 2012, Huningue, France.Enamel-renal syndrome with congenital heart defects and asthma: a rare association in a Moroccan child.MSX2 Gene Duplication in a Patient with Eye Development Defects.Dental Findings in Patients With Non-surgical Hypoparathyroidism and Pseudohypoparathyroidism: A Systematic Review.Septo-optic dysplasia, subglottic stenosis and skeletal abnormalities: a case reportThe variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndromeGalactosylceramide lipidosis (Krabbe's disease) and deciduous dental tissues. A case reportGenetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root PatterningProtocol GenoDENT: Implementation of a New NGS Panel for Molecular Diagnosis of Genetic Disorders with Orodental Involvement
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