Résultats de la recherche

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Orodental phenotype and genotype findings in all subtypes of hypophosphatasia.
A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta
Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.

Islandora displays