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

Otologic characteristics of individuals with deletions of distal 18q.

The Laryngoscope - 1 Nov 2014

Perry Brian P, Cody Jannine D

Abstract excerpt

OBJECTIVES/HYPOTHESIS: To fully describe the otologic features seen in individuals with deletions of the distal long arm of chromosome 18 (distal 18q-). STUDY DESIGN: Cross-sectional/observational. METHODS: More than 200 individuals with deletions of the long arm of chromosome 18 underwent a comp...

Read the complete abstract on PubMed

Topics

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

Share to Age Distribution
Share to Audiometry, Pure-Tone
Share to Chromosome Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cross-Sectional Studies

Share to Hearing Loss, Conductive

Share to Hearing Loss, Sensorineural

Share to Risk Assessment

Share to Sex Distribution

Source

Identifiers

PMID: 24912803
DOI: 10.1002/lary.24769

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24912803-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Otologic characteristics of individuals with deletions of distal 18q.PMID 24912803Read ↗

Identification of 2.3-Mb gene locus for congenital aural atresia in 18q22.3 deletion: a case report analyzed by comparative genomic hybridization.Semantic proximity Read ↗

Whole arm deletions of 18p: medical and developmental effects.Semantic proximity Read ↗

Establishing a reference group for distal 18q-: clinical description and molecular basis.Semantic proximity Read ↗

Narrowing critical regions and determining penetrance for selected 18q- phenotypes.Semantic proximity Read ↗

Anatomical Changes and Audiological Profile in Branchio-oto-renal Syndrome: A Literature ReviewSemantic proximity Read ↗

The 18q deletion syndrome and analysis of the critical region for orofacial cleft at 18q22.3.Semantic proximity Read ↗

Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic map.Semantic proximity Read ↗

Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability.Semantic proximity Read ↗

Craniofacial and Neurological Phenotype in a Patient with De Novo 18q Microdeletion and 18p Microduplication.Semantic proximity Read ↗

18q deletions: clinical, molecular, and brain MRI findings of 14 individuals.Semantic proximity Read ↗

Autoimmune thyroid disease and pituitary adenoma in a female patient with 18p deletion syndrome: a case report and review of the literatureSemantic proximity Read ↗

[Deletion on the short arm of chromosome 18 syndrome diagnosed by array comparative genomic hybridization. Presentation of one case with a mild phenotype].Semantic proximity Read ↗

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