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Novel NECTIN4 Mutations in Ectodermal Dysplasia Syndactyly Syndrome in Two Families.
Like Father, Like Daughter - Ectodermal Dysplasia-Syndactyly Syndrome: A Case Report.
A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family.
A novel homozygous nonsense mutation in NECTIN4 gene in a Pakistani family with ectodermal dysplasia syndactyly syndrome 1.
A Novel Pathogenic Variant of NECTIN4 Gene in a Child with Ectodermal Dysplasia-Syndactyly Syndrome.