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: hypophosphatasia - update 2013.

European journal of human genetics : EJHG - 1 Apr 2014

Mornet Etienne, Hofmann Christine, Bloch-Zupan Agnès, Girschick Hermann, Le Merrer Martine

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 Alkaline Phosphatase
Share to Alkaline Phosphatase Research Studies
Share to Biochemical and Molecular Research
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Hypophosphatasia

Share to Phenotype

Share to Vitamin D Research Studies

Source

Open in PubMed Open full text

Identifiers

PMID: 23921539
DOI: 10.1038/ejhg.2013.177
PMCID: PMC3953904

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: hypophosphatasia - update 2013.PMID 23921539Read ↗

Clinical utility gene card for: Alport syndrome - update 2014.Semantic proximity Read ↗

Hypophosphatasia update: recent advances in diagnosis and treatment.Semantic proximity Read ↗

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

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

Clinical utility gene card for: Trimethylaminuria - update 2014.Semantic proximity Read ↗

Clinical utility gene card for: Alport syndromeSemantic proximity Read ↗

A clinical and research protocol for characterizing patients with hypophosphatasia.Semantic proximity Read ↗

Clinical utility gene card for: achromatopsia.Semantic proximity Read ↗

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

Hypophosphatasia: an overview of the disease and its treatmentSemantic proximity Read ↗

Clinical utility gene card for: Aniridia.Semantic proximity Read ↗

[Molecular basis of hypophosphatasia].Semantic proximity Read ↗

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