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

Juvenile myoclonic epilepsy in chromosome 6p12-p11: locus heterogeneity and recombinations.

American journal of medical genetics - 14 Jun 1996

Liu A W, Delgado-Escueta A V, Gee M N, Serratosa J M, Zhang Q W, Alonso M E, Medina M T, Cordova S, Zhao H Z, Spellman J M, Donnadieu F R, Peek J R, Treiman L J, Sparkes R S

Abstract excerpt

We recently analyzed under homogeneity a large pedigree from Belize with classic juvenile myoclonic epilepsy (JME). After a genome wide search with 146 microsatellites, we obtained significant linkage between chromosome 6p markers, D6S257 and D6S272, and both convulsive and EEG traits of JME. Rec...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Linkage
Share to Genetic Markers
Share to Haplotypes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Phenotype

Share to Polymorphism, Genetic

Share to Recombination, Genetic

Share to Repetitive Sequences, Nucleic Acid

Source

Identifiers

PMID: 8737649
DOI: 10.1002/(SICI)1096-8628(19960614)63:3<438::AID-AJMG5>3.0.CO;2-N

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-8737649-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Juvenile myoclonic epilepsy in chromosome 6p12-p11: locus heterogeneity and recombinations.PMID 8737649Read ↗

Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy.Semantic proximity Read ↗

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.Semantic proximity Read ↗

The chromosome 6p epilepsy locus: exploring mode of inheritance and heterogeneity through linkage analysis.Semantic proximity Read ↗

Evidence for linkage between juvenile myoclonic epilepsy-related idiopathic generalized epilepsy and 6p11-12 in Dutch families.Semantic proximity Read ↗

[Juvenile myoclonic epilepsy in chromosome 6p12: clinical and genetic advances].Semantic proximity Read ↗

The quest for juvenile myoclonic epilepsy genes.Semantic proximity Read ↗

Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6Semantic proximity Read ↗

A locus for generalized tonic-clonic seizure susceptibility maps to chromosome 10q25-q26.Semantic proximity Read ↗

BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy.Semantic proximity Read ↗

Genetic susceptibility in Juvenile Myoclonic Epilepsy: Systematic review of genetic association studies.Semantic proximity Read ↗

Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy.Semantic proximity Read ↗

Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patientsSemantic proximity Read ↗

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