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Article

Benign Familial Infantile Convulsions: Mapping of a Novel Locus on Chromosome 2q24 and Evidence for Genetic Heterogeneity

1 Jun 2001

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

Identifiers

PMID: 11326335
DOI: 10.1086/320596

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Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

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Benign Familial Infantile Convulsions: Mapping of a Novel Locus on Chromosome 2q24 and Evidence for Genetic HeterogeneityPMID 11326335Read ↗

Benign familial infantile convulsions: report of a UK family and confirmation of genetic heterogeneity.Semantic proximity Read ↗

Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q.Semantic proximity Read ↗

Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity.Semantic proximity Read ↗

Novel K+ channel genes in benign familial neonatal convulsions.Semantic proximity Read ↗

Positive association between benign familial infantile convulsions and LGI4.Semantic proximity Read ↗

Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis SyndromeSemantic proximity Read ↗

[Benign familial neonatal convulsion].Semantic proximity Read ↗

[Benign familial neonatal convulsions: molecular pathology and diagnosis].Semantic proximity Read ↗

[Clinical and genetic analysis of a Chinese pedigree affected with benign familial neonatal convulsion].Semantic proximity Read ↗

Genetic and biologic classification of infantile spasms.Semantic proximity Read ↗

No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1.Semantic proximity Read ↗

Phenotypic expression of benign familial neonatal convulsions linked to chromosome 20.Semantic proximity Read ↗

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