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Article

Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia.

American journal of medical genetics. Part A - 1 Aug 2006

Neal Jason, Apse Kira, Sahin Mustafa, Walsh Christopher A, Sheen Volney L

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Share to Abnormalities, Multiple
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 1
Share to Genes, Dominant

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

Share to Genetic Techniques

Share to In Situ Hybridization, Fluorescence

Share to Nervous System Malformations

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Source

Identifiers

PMID: 16835933
DOI: 10.1002/ajmg.a.31334

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.

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Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia.PMID 16835933Read ↗

Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneitySemantic proximity Read ↗

Mutation in PQBP1 is associated with periventricular heterotopia.Semantic proximity Read ↗

Periventricular nodular heterotopias is associated with mutation at the FLNA locus-a case history and a literature review.Semantic proximity Read ↗

Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36.Semantic proximity Read ↗

Location of periventricular nodular heterotopia is related to the malformation phenotype on MRI.Semantic proximity Read ↗

Genetic causes underlying grey matter heterotopiaSemantic proximity Read ↗

Constitutional 1p36 deletion in a child with neuroblastoma.Semantic proximity Read ↗

A new 1p36.13-1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis.Semantic proximity Read ↗

Periventricular nodular heterotopia with overlying polymicrogyria.Semantic proximity Read ↗

Patient with bilateral periventricular nodular heterotopia and polymicrogyria with apparently balanced reciprocal translocation t(1;6)(p12;p12.2) that interrupts the mannosidase alpha, class 1A, and glutathione S-transferase A2 genes.Semantic proximity Read ↗

47 patients with FLNA associated periventricular nodular heterotopia.Semantic proximity Read ↗

FLNA genomic rearrangements in a 391 French bilateral periventricular nodular heterotopia cohort: prevalence and phenotypic correlations.Semantic proximity Read ↗

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