Familial case of piebaldism with regression of white forelock.

doi:10.1111/j.1365-2230.2008.02703.x

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

Community

Back to search

Article

Familial case of piebaldism with regression of white forelock.

Clinical and experimental dermatology - 1 Jul 2008

Matsunaga H, Tanioka M, Utani A, Miyachi Y

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 Genotype
Share to Infant
Share to Mutation
Share to Piebaldism

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Remission, Spontaneous

Source

Open in PubMed

Identifiers

PMID: 18355360
DOI: 10.1111/j.1365-2230.2008.02703.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial case of piebaldism with regression of white forelock.PMID 18355360Read ↗

Piebaldism.Semantic proximity Read ↗

The molecular basis of human piebaldism.Semantic proximity Read ↗

Familial radial dyplasia with renal ectopia.Semantic proximity Read ↗

Beckwith–Wiedemann syndromeSemantic proximity Read ↗

[A novel KIT gene mutation results in piebaldism].Semantic proximity Read ↗

Limb body‐wall complex in association with sirenomelia sequenceSemantic proximity Read ↗

Evidence of iris-earlobe linkage in a mosaic man.Semantic proximity Read ↗

Familial occurrence of isolated Dandy-Walker variant in two consecutive male fetuses.Semantic proximity Read ↗

Atrichia with papular lesions and mental retardation in two sisters.Semantic proximity Read ↗

[Piebaldisme: a rare genodermatosis].Semantic proximity Read ↗

Hereditary pincer nail.Semantic proximity Read ↗

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