• Case report of Schöpf-Schulz-Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A
• Clinical, genetic, epidemiologic, evolutionary, and functional delineation of <em>TSPEAR</em>-related autosomal recessive ectodermal dysplasia 14
• Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia
• Dose Dependence Effect in Biallelic <em>WNT10A</em> Variant-Associated Tooth Agenesis Phenotype
• Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation
• Odonto-onycho-dermal dysplasia syndrome
• Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia
• Recessive palmoplantar keratodermas: a tale of wings, hands, hair and cancer
• Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A
• The WNT10A gene in ectodermal dysplasias and selective tooth agenesis
• Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations
• Variability in dentofacial phenotypes in four families with WNT10A mutations
• Variant of odontoonychodermal dysplasia?
• WNT 10A-mutations as explanation for tooth agenesis
• WNT10A and isolated hypodontia
• WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome
• WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes