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

Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.

American journal of human genetics - 1 Oct 1997

Jarman P R, Wood N W, Davis M T, Davis P V, Bhatia K P, Marsden C D, Davis M B

Abstract excerpt

Hereditary geniospasm is an unusual movement disorder causing episodes of involuntary tremor of the chin and the lower lip. Episodes typically start in early childhood and may be precipitated by stress, concentration, and emotion. Hereditary geniospasm is inherited as an autosomal dominant trait, and its cause is not known. We report the results of a genomewide genetic linkage study in a four-generation British...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child, Preschool
Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Dominant

Share to Genetic Linkage

Share to Genetic Markers

Share to Lod Score

Share to Pedigree

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 9382105
DOI: 10.1086/514883
PMCID: PMC1715984

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.PMID 9382105Read ↗

A genetic linkage study in Brazil identifies a new locus for persistent developmental stuttering on chromosome 10.Semantic proximity Read ↗

Novel mental retardation-epilepsy syndrome linked to Xp21.1-p11.4.Semantic proximity Read ↗

A gene for ataxic cerebral palsy maps to chromosome 9p12-q12.Semantic proximity Read ↗

A high-resolution linkage map of human 9q34.1.Semantic proximity Read ↗

Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31.Semantic proximity Read ↗

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.Semantic proximity Read ↗

Familial paroxysmal kinesigenic choreoathetosis: an electrophysiologic and genotypic analysis.Semantic proximity Read ↗

Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1.Semantic proximity Read ↗

An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian family.Semantic proximity Read ↗

Novel genetic findings in an extended family pedigree with sleepwalking.Semantic proximity Read ↗

Genetic studies of stuttering in a founder population.Semantic proximity Read ↗

Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q.Semantic proximity Read ↗

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