Résultats de la recherche

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Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar.
Corrigendum: Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar
A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.

Islandora displays