Discover Community Create You

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

Article

A compound nucleotide repeat in the neurofibromatosis (NF1) gene.

Human molecular genetics - 1 Jul 1993

Andersen L B, Tarlé S A, Marchuk D A, Legius E, Collins F S

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 Alleles
Share to Base Sequence
Share to Chromosomes, Human, Pair 17
Share to DNA

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

Share to Gene Frequency

Share to Genes, Neurofibromatosis 1

Share to Oligodeoxyribonucleotides

Share to Repetitive Sequences, Nucleic Acid

Source

Identifiers

PMID: 8364559
DOI: 10.1093/hmg/2.7.1083-a

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A compound nucleotide repeat in the neurofibromatosis (NF1) gene.PMID 8364559Read ↗

Novel human pathological mutations. Gene symbol: NF1. Disease: neurofibromatosis 1.Semantic proximity Read ↗

Six novel mutations in the neurofibromatosis type 1 (NF1) gene.Semantic proximity Read ↗

A novel neurofibromatosis type 1 (NF1) mutation in a patient with NF1 and pheochromocytoma.Semantic proximity Read ↗

Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients.Semantic proximity Read ↗

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

Ten base pair duplication in exon 38 of the NF1 gene.Semantic proximity Read ↗

Two novel mutations of NF1 gene identified in Chinese patients with severe neurofibromatosis type 1.Semantic proximity Read ↗

Molecular basis of neurofibromatosis type 1 (NF1): mutation analysis and polymorphisms in the NF1 gene.Semantic proximity Read ↗

The neurofibromatosis type 1 gene.Semantic proximity Read ↗

A de novo Alu insertion results in neurofibromatosis type 1.Semantic proximity Read ↗

Homonucleotide tracts, short repeats and CpG/CpNpG motifs are frequent sites for heterogeneous mutations in the neurofibromatosis type 1 (NF1) tumour-suppressor gene.Semantic proximity Read ↗

An Alu polymorphism intragenic to the neurofibromatosis type 1 gene (NF1).Semantic proximity Read ↗

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