Reviewing the Genetic and Molecular Foundations of Congenital Spinal Deformities: Implications for Classification and Diagnosis. [PDF]
Samarkhanova D, Zhabagin M, Nadirov N.
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Familial Tooth Agenesis in Lebanese Patients: Clinical Characterization and Whole-Exome Identification of Rare CACNA2D2 and TRIO Variants. [PDF]
Nabbout F +3 more
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Evolution of cetacean-specific conserved non-coding elements suggests their role in the limb changes during secondary aquatic adaptation. [PDF]
Zhang Z +7 more
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A novel PAX9 variant in a Chinese family with non-syndromic oligodontia and genotype-phenotype analysis of PAX9variants. [PDF]
Jin Z +14 more
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What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndromic hypodontia? A case-control study in orthodontically treated patients. [PDF]
Alhazmi N +7 more
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Fabrication of Hard Tissue Constructs from Induced Pluripotent Stem Cells for Exploring Mechanisms of Hereditary Tooth/Skeletal Dysplasia. [PDF]
Kondo T +8 more
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Physiologic and molecular effects of alcohol in the esophagus: a narrative review. [PDF]
Shaker A.
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Dissecting the role of epigenetic regulation in oral squamous cell carcinoma microenvironment: mechanisms and therapeutics. [PDF]
Li X +5 more
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Loxl3 Affects Palatal Shelf Elevation by Regulating Cell Proliferation and Collagen Deposition. [PDF]
Liu Z +5 more
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Mutations in the PAX9 gene in sporadic oligodontia
Orthodontics and Craniofacial Research, 2010Oligodontia, a congenital lack of six or more teeth, is often associated with mutations in the PAX9 gene; therefore, we searched for mutations in this gene.In the present work, we sequenced fragments of the PAX9 gene in individuals with sporadic oligodontia. Next, we genotyped some mutations we found in patients with oligodontia and individuals without
Tomasz Poplawski
exaly +6 more sources

