Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Phenotypic findings in Chinese families with X-linked hypohydrotic ectodermal dysplasia.

Archives of oral biology - 1 Oct 2012

Yin Wei, Ye XiaoQian, Bian Zhuan

Abstract excerpt

OBJECTIVE: To summarize the phenotypic characters of Chinese X-linked hypohidrotic ectodermal dysplasia (XLHED) subjects. DESIGN: Twelve affected and 24 carriers from seven Chinese pedigrees were recruited. The development of their hair, tooth, skin and sweat gland was (semi-)quantitatively evaluated. From 100 to 250 normal controls were used to exclude polymorphisms in each family. RESULTS: Different from the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged, 80 and over
Share to Case-Control Studies
Share to Chi-Square Distribution

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

Share to Child, Preschool

Share to Ectodermal Dysplasia 1, Anhidrotic

Share to Pedigree

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 22633615
DOI: 10.1016/j.archoralbio.2012.03.010

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Phenotypic findings in Chinese families with X-linked hypohydrotic ectodermal dysplasia.PMID 22633615Read ↗

Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

Mutation Screening of the EDA Gene in Seven Chinese Families with X-Linked Hypohidrotic Ectodermal Dysplasia.Semantic proximity Read ↗

No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study.Semantic proximity Read ↗

Novel EDA mutation in X-linked hypohidrotic ectodermal dysplasia and genotype-phenotype correlation.Semantic proximity Read ↗

[Hypohidrotic ectodermal dysplasia syndrome. Description of a clinical case].Semantic proximity Read ↗

A novel STS mutation and an Xp22.3 microdeletion from one Chinese family with X-linked ichthyosisSemantic proximity Read ↗

[Genetic testing and genotype-phenotype analysis for a child with X-linked hypohidrotic ectodermal dysplasia].Semantic proximity Read ↗

Characterization of X-linked hypohidrotic ectodermal dysplasia (XL-HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging.Semantic proximity Read ↗

A compound heterozygous mutation in the EDAR gene in a Spanish family with autosomal recessive hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings.Semantic proximity Read ↗

X-linked hypohidrotic ectodermal dysplasia. Genetic and dental findings in 67 Danish patients from 19 families.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.