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 features of type 2 Stickler syndrome.

Journal of medical genetics - 1 Aug 2004

Poulson A V, Hooymans J M M, Richards A J, Bearcroft P, Murthy R, Baguley D M, Scott J D, Snead M P

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 Abnormalities, Multiple
Share to Aged, 80 and over
Share to Collagen Type XI
Share to Connective Tissue Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Osteochondrodysplasias

Share to Pedigree

Share to Retinal Detachment

Share to Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 15286167
DOI: 10.1136/jmg.2004.018382
PMCID: PMC1735871

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 features of type 2 Stickler syndrome.PMID 15286167Read ↗

Stickler syndrome.Semantic proximity Read ↗

Clinical Variability of Stickler SyndromeSemantic proximity Read ↗

Stickler syndrome type 1: case series and new genetic variantsSemantic proximity Read ↗

Distinguishing Marshall from Stickler syndrome: a clinical and genetic challenge.Semantic proximity Read ↗

Stickler syndrome: clinical characteristics and diagnostic criteria.Semantic proximity Read ↗

Stickler Syndrome.Semantic proximity Read ↗

Hypoplasic Vitreous in Stickler Syndrome.Semantic proximity Read ↗

A novel mutation in the COL2A1 gene in a patient with Stickler syndrome type 1: a case report and review of the literature.Semantic proximity Read ↗

Atypical presentation of Waardenburg's syndrome type II.Semantic proximity Read ↗

The Stickler syndrome: genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1.Semantic proximity Read ↗

Clinical and molecular genetics of Stickler syndromeSemantic proximity Read ↗

What is Kindler syndrome?Semantic proximity Read ↗

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