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

Clinical utility gene card for: Alport syndrome - update 2014.

European journal of human genetics : EJHG - 1 Sept 2015

Hertz Jens Michael, Thomassen Mads, Storey Helen, Flinter Frances

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 Autoantigens
Share to Collagen Type IV
Share to Gene Expression
Share to Genes, Recessive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Incidence

Share to Nephritis, Hereditary

Share to Sex Factors

Share to United Kingdom

Source

Open in PubMed Open full text

Identifiers

PMID: 25388007
DOI: 10.1038/ejhg.2014.254
PMCID: PMC4538213

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical utility gene card for: Alport syndrome - update 2014.PMID 25388007Read ↗

Clinical utility gene card for: Alport syndromeSemantic proximity Read ↗

Clinical utility gene card for: 3-M syndrome - update 2013.Semantic proximity Read ↗

Clinical utility gene card for: CHARGE syndrome - update 2015.Semantic proximity Read ↗

Clinical utility gene card for: Zellweger syndrome spectrum.Semantic proximity Read ↗

Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII and variants - update 2012.Semantic proximity Read ↗

Molecular diagnosis of Alport syndrome: the experience in Siena.Semantic proximity Read ↗

Clinical utility gene card for: Alagille Syndrome (ALGS)Semantic proximity Read ↗

Clinical utility gene card for: hypophosphatasia - update 2013.Semantic proximity Read ↗

Alport syndrome: facts and opinionsSemantic proximity Read ↗

[Current developments in the diagnosis of Alport syndrome].Semantic proximity Read ↗

Clinical utility gene card for: Fabry disease.Semantic proximity Read ↗

Clinical utility gene card for: Meckel syndrome - update 2016.Semantic proximity Read ↗

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