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

Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications

26 Aug 2014

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 Epilepsy research and treatment
Share to Genomic variations and chromosomal abnormalities
Share to Genomics and Rare Diseases

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25172301
DOI: 10.1016/j.braindev.2014.08.002

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

Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complicationsPMID 25172301Read ↗

Identification of proximal 1p36 deletions using array‐CGH: a possible new syndromeSemantic proximity Read ↗

1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients.Semantic proximity Read ↗

[1p36 microdeletion syndrome].Semantic proximity Read ↗

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.Semantic proximity Read ↗

Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions.Semantic proximity Read ↗

1p36 deletion syndrome associated with Prader-Willi-like phenotype.Semantic proximity Read ↗

Population data suggest that deletions of 1p36 are a relatively common chromosome abnormalitySemantic proximity Read ↗

Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the SyndromeSemantic proximity Read ↗

Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.Semantic proximity Read ↗

Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of CardiomyopathySemantic proximity Read ↗

Inverted duplication of 1q32.1 to 1q44 characterized by array CGH and review of distal 1q partial trisomy.Semantic proximity Read ↗

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

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