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

Subcortical Band Heterotopia in Rare Affected Males Can be Caused by Missense Mutations in DCX (XLIS) or LIS1

1 Sept 1999

Abstract excerpt

Subcortical band heterotopia (SBH) are bilateral and symmetric ribbons of gray matter found in the central white matter between the cortex and the ventricular surface, which comprises the less severe end of the lissencephaly (agyria-pachygyria-band) spectrum of malformations. Mutations in DCX (also known as XLIS ) have previously been described in females with SBH. We have now identified mutations in either the...

Read the complete abstract on PubMed

Topics

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

Share to Cerebrospinal fluid and hydrocephalus
Share to Fetal and Pediatric Neurological Disorders
Share to Neonatal and fetal brain pathology

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 10441340
DOI: 10.1093/hmg/8.9.1757

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Subcortical Band Heterotopia in Rare Affected Males Can be Caused by Missense Mutations in DCX (XLIS) or LIS1PMID 10441340Read ↗

Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females.Semantic proximity Read ↗

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.Semantic proximity Read ↗

Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis.Semantic proximity Read ↗

Genotype-phenotype correlation in lissencephaly and subcortical band heterotopia: the key questions answered.Semantic proximity Read ↗

Mosaic mutations of the <i>LIS1</i> gene cause subcortical band heterotopiaSemantic proximity Read ↗

Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia.Semantic proximity Read ↗

The location of DCX mutations predicts malformation severity in X-linked lissencephaly.Semantic proximity Read ↗

[A male case of subcortical band heterotopia with somatic mosaicism of DCX mutation].Semantic proximity Read ↗

New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum.Semantic proximity Read ↗

Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary.Semantic proximity Read ↗

Identification of DCX gene mutation in lissencephaly spectrum with subcortical band heterotopia using whole exome sequencing.Semantic proximity Read ↗

Novel DCX mutation-caused lissencephaly in a boy and very mild heterotopia in his mother.Semantic proximity Read ↗

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