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: 16p13.11 microdeletion syndrome.

European journal of human genetics : EJHG - 1 May 2014

Tropeano Maria, Andrieux Joris, 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 Amidohydrolases
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 16
Share to Diagnosis, Differential

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Counseling

Share to Microtubule-Associated Proteins

Share to Prenatal Diagnosis

Share to Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 24105370
DOI: 10.1038/ejhg.2013.230
PMCID: PMC3992581

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 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: 16p13.11 microdeletion syndrome.PMID 24105370Read ↗

Clinical utility gene card for: 15q13.3 microdeletion syndrome.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: mucopolysaccharidosis type II.Semantic proximity Read ↗

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

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

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

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

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

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

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

Clinical utility gene card for: Rothmund-Thomson syndrome.Semantic proximity Read ↗

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