Neonatal Marfan Syndrome by Inherited Mutation.

doi:10.1007/s12098-020-03411-y

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

Neonatal Marfan Syndrome by Inherited Mutation.

Indian journal of pediatrics - 1 Feb 2021

Mastromoro Gioia, Guida Valentina, Cellitti Raffaella, Cardilli Viviana, De Luca Alessandro, Pizzuti Antonio, Versacci Paolo

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 Infant, Newborn
Share to Marfan Syndrome
Share to Microfilament Proteins
Share to Musculoskeletal Abnormalities

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

Share to Mutation

Share to Phenotype

Source

Open in PubMed

Identifiers

PMID: 32557139
DOI: 10.1007/s12098-020-03411-y

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 9 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Neonatal Marfan Syndrome by Inherited Mutation.PMID 32557139Read ↗

Genes and gene products involved in Marfan syndrome.Semantic proximity Read ↗

Genetic testing in Marfan syndrome.Semantic proximity Read ↗

Neonatal Marfan syndrome: unusually large deletion of exons 24-26 of FBN1 associated with poor prognosis.Semantic proximity Read ↗

[Case of congenital Marfan's syndrome].Semantic proximity Read ↗

Familial neonatal Marfan syndrome due to parental mosaicism of a missense mutation in the <i>FBN1</i> geneSemantic proximity Read ↗

An unusual patient with the neonatal Marfan phenotype and mitochondrial complex I deficiency.Semantic proximity Read ↗

Recent progress in genetics of Marfan syndrome and Marfan-associated disordersSemantic proximity Read ↗

Marfan syndrome with a homozygous FBN1 splicing mutation.Semantic proximity Read ↗

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