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

[Gene responsible for Waardenburg syndrome type I].

Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme - 1 Feb 1993

Tsukamoto K, Niikawa N

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 Chromosome Mapping
Share to Chromosomes, Human, Pair 2
Share to Cosmids
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Share to Restriction Mapping

Share to Waardenburg Syndrome

Source

Identifiers

PMID: 8098159

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Gene responsible for Waardenburg syndrome type I].PMID 8098159Read ↗

[Waardenburg syndrome].Semantic proximity Read ↗

[Werner's syndrome and aging genes].Semantic proximity Read ↗

[Werner syndrome].Semantic proximity Read ↗

[Werner syndrome].Semantic proximity Read ↗

[Molecular basis of human hereditary diseases].Semantic proximity Read ↗

[Molecular genetic understanding of hereditary disorders].Semantic proximity Read ↗

[Werner's syndrome].Semantic proximity Read ↗

[A novel mutation in Mitf gene leads to a patient with Waardenburg syndrome type II].Semantic proximity Read ↗

A family with Waardenburg syndrome.Semantic proximity Read ↗

[Aarskog-Scott syndrome].Semantic proximity Read ↗

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

[Mutation analysis of seven patients with Waardenburg syndrome].Semantic proximity Read ↗

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