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

Intra-familial variability of ectodermal defects associated with WNT10A mutations.

Acta dermato-venereologica - 1 May 2011

Wedgeworth Emma K, Nagy Nikoletta, White Jonathan M L, Pembroke Andrew C, McGrath John A

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to DNA Mutational Analysis
Share to Ectodermal Dysplasia
Share to Hair
Share to Heterozygote

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homozygote

Share to Wnt Proteins

Source

Identifiers

PMID: 21279306
DOI: 10.2340/00015555-1028

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Intra-familial variability of ectodermal defects associated with WNT10A mutations.PMID 21279306Read ↗

Phenotypic variability associated with WNT10A nonsense mutations.Semantic proximity Read ↗

Variability in dentofacial phenotypes in four families with WNT10A mutations.Semantic proximity Read ↗

Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.Semantic proximity Read ↗

WNT10A, dermatology and dentistry.Semantic proximity Read ↗

Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.Semantic proximity Read ↗

WNT10A mutations causing oligodontiaSemantic proximity Read ↗

A retrospective study of clinical and mutational findings in 45 Danish families with ectodermal dysplasia.Semantic proximity Read ↗

WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI).Semantic proximity Read ↗

Schöpf-Schulz-Passarge syndrome associated with two new missense mutations in WNT10A.Semantic proximity Read ↗

WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.Semantic proximity Read ↗

WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.Semantic proximity Read ↗

Intra-familial variation in clinical manifestations and response to ephedrine in siblings with congenital myasthenic syndrome caused by novel COLQ mutations.Semantic proximity Read ↗

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