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

Collagenopathy with a phenotype resembling Silver-Russell syndrome phenotype.

American journal of medical genetics. Part A - 1 Oct 2013

Cianci Paola, Paterlini Giuseppe, Tagliabue Paolo, Verderio Maria, Vergani Patrizia, Bianchi Maria Luisa, Giussani Carlo, Kullmann Gaia, Mazzoleni Fabio, Bozzetti Alberto, Selicorni Angelo

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 Bone and Bones
Share to Facies
Share to Infant, Newborn
Share to Magnetic Resonance Imaging

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pregnancy

Share to Radiography

Share to Silver-Russell Syndrome

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 23918677
DOI: 10.1002/ajmg.a.36093

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Collagenopathy with a phenotype resembling Silver-Russell syndrome phenotype.PMID 23918677Read ↗

Heritable collagen disorders: from genotype to phenotype.Semantic proximity Read ↗

The collagenopathies: review of clinical phenotypes and molecular correlations.Semantic proximity Read ↗

The next generation of Silver-Russell syndrome.Semantic proximity Read ↗

Silver syndrome.Semantic proximity Read ↗

[Silver-Russell syndrome].Semantic proximity Read ↗

Temple syndrome misdiagnosed as Silver-Russell syndrome.Semantic proximity Read ↗

Mutations in type IV collagen genes and Alport phenotypes.Semantic proximity Read ↗

Absent digit in Russell-Silver syndrome: expanding the clinical spectrum of a well known syndrome.Semantic proximity Read ↗

Alport syndrome: clinical and genetic correlation in a type-IV collagen disease.Semantic proximity Read ↗

Silver–Russell syndromeSemantic proximity Read ↗

Heritable Collagen Disorders: The Paradigm of the Ehlers—Danlos SyndromeSemantic proximity Read ↗

Premature arthritis is a distinct type II collagen phenotype: comment on the article by Kannu et al.Semantic proximity Read ↗

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