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Article

A family with Waardenburg syndrome.

The Journal of dermatology - 1 May 2004

Denli Yasar Gül, Yücel Aydin, Günasti Suhan, Homan Seydo, Durdu Murat, Süleymanova Dilara

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

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Identifiers

PMID: 15187316
DOI: 10.1111/j.1346-8138.2004.tb00700.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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A family with Waardenburg syndrome.PMID 15187316Read ↗

[Waardenburg syndrome].Semantic proximity Read ↗

Genetic and phenotypic heterogeneity in two novel cases of Waardenburg syndrome type IV.Semantic proximity Read ↗

Waardenburg syndrome: variable phenotypic expression in monozygotic twins.Semantic proximity Read ↗

[Gene responsible for Waardenburg syndrome type I].Semantic proximity Read ↗

Werner syndrome: molecular genetics and mechanistic hypotheses.Semantic proximity Read ↗

Three novel PAX3 mutations observed in patients with Waardenburg syndrome type 1.Semantic proximity Read ↗

Possible homozygous Waardenburg syndrome in a fetus with exencephaly.Semantic proximity Read ↗

[Aarskog-Scott syndrome].Semantic proximity Read ↗

Case of Waardenburg Shah syndrome in a family with review of literatureSemantic proximity Read ↗

Atypical presentation of Waardenburg's syndrome type II.Semantic proximity Read ↗

[Clinical classification and genetic mutation study of two pedigrees with type II Waardenburg syndrome].Semantic proximity Read ↗

Phenotypic diversity and genetic complexity of PAX3-related Waardenburg syndrome.Semantic proximity Read ↗

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