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Article

Repeat polymorphisms in human fibrillin genes on chromosome 15 (FBN1) and chromosome 5 (FBN2).

Human molecular genetics - 1 Aug 1993

Biddinger A L, Hecht J T, Milewicz D M

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Share to Chromosomes, Human, Pair 15
Share to Chromosomes, Human, Pair 5
Share to DNA Primers
Share to Fibrillin-1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Marfan Syndrome

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Share to Repetitive Sequences, Nucleic Acid

Source

Identifiers

PMID: 8401518
DOI: 10.1093/hmg/2.8.1323

Genes

FBN1
FBN2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

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Repeat polymorphisms in human fibrillin genes on chromosome 15 (FBN1) and chromosome 5 (FBN2).PMID 8401518Read ↗

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Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders.Semantic proximity Read ↗

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Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.Semantic proximity Read ↗

Five bovine polymorphic dinucleotide microsatellite markers: FBN5, FBN16, FBN17, FBN18, and FBN19.Semantic proximity Read ↗

Mutation screening of all 65 exons of the fibrillin-1 gene in 60 patients with Marfan syndrome: report of 12 novel mutations.Semantic proximity Read ↗

Software and database for the analysis of mutations in the human FBN1 geneSemantic proximity Read ↗

Differential allelic expression of a fibrillin gene (FBN1) in patients with Marfan syndrome.Semantic proximity Read ↗

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De novo heterozygous FBN1 mutations in the extreme C-terminal region cause progeroid fibrillinopathy.Semantic proximity Read ↗

Fibrillin I gene polymorphism is associated with tall stature of normal individuals.Semantic proximity Read ↗

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