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John Wiley & Sons Inc

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Identification by whole‐exome sequencing of novel mutation c.64C > G in the BTK gene of a fetus with X‐linked agammaglobulinemia

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John Wiley & Sons Inc

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X-Linked Hypohidrotic Ectodermal Dysplasia: New Features and a Novel EDA Gene Mutation

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Karger

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Case of X‐linked hypohidrotic ectodermal dysplasia with a novel EDA missense mutation

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Novel EDA mutation in X‐linked hypohidrotic ectodermal dysplasia and genotype–phenotype correlation

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