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Article

Autosomal recessive inheritance of hypohidrotic ectodermal dysplasia.

Pediatric dermatology - 1 Sept 1990

Kiss P, Török E

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 2247394
DOI: 10.1111/j.1525-1470.1990.tb00291.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Autosomal recessive inheritance of hypohidrotic ectodermal dysplasia.PMID 2247394Read ↗

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Ectodermal Dysplasia: A Genetic ReviewSemantic proximity Read ↗

Anhidrotic ectodermal dysplasia: a new mutation.Semantic proximity Read ↗

Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder.Semantic proximity Read ↗

Ectodermal dysplasias: an overview and update of clinical and molecular-functional mechanisms.Semantic proximity Read ↗

EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature.Semantic proximity Read ↗

Ocular and non-ocular manifestations of hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

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