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Article

Pitfalls in clinical diagnosis of female carriers of X-linked hypohidrotic ectodermal dysplasia.

Archives of dermatology - 1 Sept 2002

Vincent Marie-Claire, Cossée Mireille, Vabres Pierre, Stewart Fiona, Bonneau Dominique, Calvas Patrick

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Share to Biopsy, Needle
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12225002
DOI: 10.1001/archderm.138.9.1256

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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.

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Pitfalls in clinical diagnosis of female carriers of X-linked hypohidrotic ectodermal dysplasia.PMID 12225002Read ↗

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Prenatal sonographic diagnosis of X-linked hypohidrotic ectodermal dysplasia: An unusual case.Semantic proximity Read ↗

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X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient.Semantic proximity Read ↗

An uncommon case of a female carrier of two distinct X-linked disorders.Semantic proximity Read ↗

Prenatal Genetic Testing for X-Linked Hypohidrotic Ectodermal Dysplasia.Semantic proximity Read ↗

46XY girls: the importance of careful newborn examination.Semantic proximity Read ↗

Autosomal-dominant hypohidrotic ectodermal dysplasia caused by a novel mutation.Semantic proximity Read ↗

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