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Article

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

1 Jul 1991

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

Identifiers

PMID: 1852206
DOI: 10.1038/352330a0

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genesPMID 1852206Read ↗

Clinical and genetic associations in Marfan syndrome and related disorders.Semantic proximity Read ↗

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

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A second locus for Marfan syndrome maps to chromosome 3p24.2–p25Semantic proximity Read ↗

Fibrillln mutations in Marfan syndrome and related phenotypes.Semantic proximity Read ↗

Genotype-phenotype correlations of marfan syndrome and related fibrillinopathies: Phenomenon and molecular relevanceSemantic proximity Read ↗

The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2.Semantic proximity Read ↗

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