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Article

Ten base pair duplication in exon 38 of the NF1 gene.

Human molecular genetics - 1 May 1994

Legius E, Hall B K, Wallace M R, Collins F S, Glover T W

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Source

Identifiers

PMID: 8081372
DOI: 10.1093/hmg/3.5.829

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Ten base pair duplication in exon 38 of the NF1 gene.PMID 8081372Read ↗

Genomic organization and evolution of the NF1 microdeletion region☆Semantic proximity Read ↗

Characterization of six mutations in exon 37 of neurofibromatosis type 1 gene.Semantic proximity Read ↗

Characterisation of a novel splice donor mutation affecting position +1 in intron 18 of the NF-1 gene.Semantic proximity Read ↗

Characterization of NF1 allele containing two nonsense mutations in exon 37 that segregates with neurofibromatosis type 1.Semantic proximity Read ↗

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Genomic analysis of a NF1 -related pseudogene on human chromosome 21Semantic proximity Read ↗

A compound nucleotide repeat in the neurofibromatosis (NF1) gene.Semantic proximity Read ↗

Identification of two novel mutations in the NF1 gene in Chinese patients with neurofibromatosis type 1.Semantic proximity Read ↗

Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain.Semantic proximity Read ↗

Breakpoint characterization of a novel NF1 multiexonic deletion: a case showing expression of the mutated allele.Semantic proximity Read ↗

Two NF1 mutations: frameshift in the GAP-related domain, and loss of two codons toward the 3' end of the gene.Semantic proximity Read ↗

Identification of two novel mutations (1448delA and Q682X) in the NF1 gene and analysis for nonsense mutations in patients with neurofibromatosis type 1.Semantic proximity Read ↗

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