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

Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity

25 Jan 2019

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Fetal and Pediatric Neurological Disorders
Share to Prenatal Screening and Diagnostics
Share to Tumors and Oncological Cases

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 30683929
DOI: 10.1038/s41431-019-0335-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneityPMID 30683929Read ↗

Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia.Semantic proximity Read ↗

De novo and inherited private variants in MAP1B in periventricular nodular heterotopia.Semantic proximity Read ↗

Genetic causes underlying grey matter heterotopiaSemantic proximity Read ↗

Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformation.Semantic proximity Read ↗

Genetic analysis of periventricular nodular heterotopia 7 caused by a novel NEDD4L missense mutation: Case and literature summary.Semantic proximity Read ↗

Periventricular nodular heterotopia with overlying polymicrogyria.Semantic proximity Read ↗

Sporadic periventricular nodular heterotopia: Classification, phenotype and correlation with Filamin A mutations.Semantic proximity Read ↗

Correlation between mild fetal ventriculomegaly, chromosomal abnormalities, and copy number variationsSemantic proximity Read ↗

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

Phenotypic manifestations in FLNA-related periventricular nodular heterotopia: a case report and review of the literature.Semantic proximity Read ↗

A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal MigrationSemantic proximity Read ↗

Rare copy number variation in cerebral palsySemantic proximity Read ↗

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