Marfan syndrome database information unreliable for diagnoses.

doi:10.1002/ajmg.a.37195

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

Community

Back to search

Article

Marfan syndrome database information unreliable for diagnoses.

American journal of medical genetics. Part A - 1 Jul 2015

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 Databases, Genetic
Share to Fibrillins
Share to Genetic Association Studies
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetics, Medical

Share to Marfan Syndrome

Share to Microfilament Proteins

Source

Open in PubMed

Identifiers

PMID: 26097176
DOI: 10.1002/ajmg.a.37195

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 10 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Marfan syndrome database information unreliable for diagnoses.PMID 26097176Read ↗

Diagnosis and treatment of Marfan syndrome: an update.Semantic proximity Read ↗

Difficulties in diagnosing Marfan syndrome using current FBN1 databases.Semantic proximity Read ↗

Guidelines for the Diagnosis and Management of Marfan SyndromeSemantic proximity Read ↗

[Marfan syndrome].Semantic proximity Read ↗

New guidelines for diagnosis of Marfan and Loey-Dietz syndromes.Semantic proximity Read ↗

Evaluating the quality of Marfan genotype-phenotype correlations in existing FBN1 databases.Semantic proximity Read ↗

Marfan gene discovered.Semantic proximity Read ↗

Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1].Semantic proximity Read ↗

Challenges in the diagnosis of Marfan syndrome.Semantic proximity Read ↗

Prevalence, incidence, and age at diagnosis in Marfan SyndromeSemantic proximity Read ↗

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