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: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches.

European journal of human genetics : EJHG - 1 Apr 2017

Richardson Rose, Sowden Jane, Gerth-Kahlert Christina, Moore Anthony T, Moosajee Mariya

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 Genetic Predisposition to Disease
Share to Genetic Testing
Share to Genome-Wide Association Study

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to High-Throughput Nucleotide Sequencing

Share to Microphthalmos

Share to Whole Genome Sequencing

Source

Open in PubMed Open full text

Identifiers

PMID: 28098148
DOI: 10.1038/ejhg.2016.201
PMCID: PMC5386421

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 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: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches.PMID 28098148Read ↗

CUGC for syndromic microphthalmia including next-generation sequencing-based approaches.Semantic proximity Read ↗

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

Clinical utility gene card for: HMSN/HNPP HMSN types 1, 2, 3, 6 (CMT1,2,4, DSN, CHN, GAN, CCFDN, HNA); HNPP.Semantic proximity Read ↗

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

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

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

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

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

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

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

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

Clinical utility gene card for: von Hippel-Lindau (VHL).Semantic proximity Read ↗

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