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

[DNA duplication in hereditary type Ia motor and sensory neuropathy (Charcot-Marie-Tooth disease)].

Nederlands tijdschrift voor geneeskunde - 21 Dec 1991

Hoogendijk J E, Baas F, de Visser M, Bolhuis P A

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 Charcot-Marie-Tooth Disease
Share to Chromosome Aberrations
Share to Chromosomes, Human, Pair 17

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

Share to Genetic Counseling

Share to Genetic Markers

Share to Mutation

Source

Identifiers

PMID: 1758499

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

[DNA duplication in hereditary type Ia motor and sensory neuropathy (Charcot-Marie-Tooth disease)].PMID 1758499Read ↗

An inherited DNA rearrangement and gene dosage effect are responsible for the most common autosomal dominant peripheral neuropathy: Charcot-Marie-Tooth disease type 1A.Semantic proximity Read ↗

Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A.Semantic proximity Read ↗

Charcot-Marie-Tooth polyneuropathy: duplication, gene dosage, and genetic heterogeneity.Semantic proximity Read ↗

[The diagnosis and prevalence of locus CMT1A duplication in Charcot-Marie-Tooth disease type 1].Semantic proximity Read ↗

[Analysis of mutations in the chromosome 17p11.2 region in patients with Charcot-Marie-Tooth type 1 disease and in patients with tomaculous neuropathy].Semantic proximity Read ↗

[Analysis of heterozygous duplication of PMP22 gene in a pedigree affected with Charcot Marie Tooth disease].Semantic proximity Read ↗

[Clinical, pathologic and molecular genetic studies of patients with hereditary motor and sensory neuropathy (HMSN)].Semantic proximity Read ↗

Duplication analysis in Turkish Charcot-Marie-Tooth type 1A patients using short tandem repeat markers.Semantic proximity Read ↗

[Phenotypic heterogeneity in Japanese Charcot-Marie-Tooth disease type 1A patients with PMP-22 gene duplication].Semantic proximity Read ↗

Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a).Semantic proximity Read ↗

De-novo mutation in hereditary motor and sensory neuropathy type I.Semantic proximity Read ↗

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A.Semantic proximity Read ↗

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