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: 15q13.3 microdeletion syndrome.

European journal of human genetics : EJHG - 1 Nov 2014

Tropeano Maria, Andrieux Joris, Vassos Evangelos, Collier David A

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 alpha7 Nicotinic Acetylcholine Receptor
Share to Chromosome Disorders
Share to Chromosomes, Human, Pair 15
Share to Endodeoxyribonucleases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Exodeoxyribonucleases

Share to Kruppel-Like Transcription Factors

Share to Multifunctional Enzymes

Share to Seizures

Source

Open in PubMed Open full text

Identifiers

PMID: 24824131
DOI: 10.1038/ejhg.2014.88
PMCID: PMC4200442

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: 15q13.3 microdeletion syndrome.PMID 24824131Read ↗

Clinical utility gene card for: 16p13.11 microdeletion syndrome.Semantic proximity Read ↗

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

Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype.Semantic proximity Read ↗

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

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

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

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

Chromosome 15q24 microdeletion syndromeSemantic proximity Read ↗

Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches.Semantic proximity Read ↗

Clinical utility gene card for: Angelman Syndrome.Semantic proximity Read ↗

Clinical utility gene card for: mucopolysaccharidosis type II.Semantic proximity Read ↗

Delineation of 15q13.3 microdeletions.Semantic proximity Read ↗

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