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

Analysis of auditory phenotype and karyotype in 200 females with Turner syndrome.

Ear and hearing - 1 Dec 2007

King Kelly A, Makishima Tomoko, Zalewski Christopher K, Bakalov Vladimir K, Griffith Andrew J, Bondy Carolyn A, Brewer Carmen C

Abstract excerpt

OBJECTIVES: Turner syndrome is the most common sex chromosome disorder in females, and is caused by a total or partial deletion of one X chromosome. The purpose of this study was to describe the auditory phenotype in a large group of individuals with Turner Syndrome, with analysis focusing on hearing loss and age, as well as the phenotypic relationship to karyotype variation. DESIGN: Our analysis of auditory...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child
Share to Chromosome Deletion

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

Share to Chromosomes, Human, X

Share to Gene Frequency

Share to Hearing

Share to Karyotyping

Share to Turner Syndrome

Source

Identifiers

PMID: 17982369
DOI: 10.1097/AUD.0b013e318157677f

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of auditory phenotype and karyotype in 200 females with Turner syndrome.PMID 17982369Read ↗

Alport syndrome: clinical update.Semantic proximity Read ↗

Hearing loss in Turner syndrome.Semantic proximity Read ↗

Karyotype-Phenotype Correlation in Turner Syndrome at a Single Center in Eastern India.Semantic proximity Read ↗

The Turner syndrome life course project: Karyotype-phenotype analyses across the lifespan.Semantic proximity Read ↗

New approach to phenotypic variability and karyotype-phenotype correlation in Turner syndrome.Semantic proximity Read ↗

Unbalanced X;14 Translocation Leading to Turner Syndrome Phenotype: a case report and review of literatureSemantic proximity Read ↗

Turner Syndrome Genotype and Phenotype and Their Effect on Presenting Features and Timing of DiagnosisSemantic proximity Read ↗

Karyotype-phenotype associations in turner syndrome: a multicenter retrospective cohort study.Semantic proximity Read ↗

Revisiting the Neuropsychological and Clinical Profile of Mosaic Turner Syndrome With a Ring X Chromosome.Semantic proximity Read ↗

X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical care.Semantic proximity Read ↗

Genomic imprinting in Turner syndrome: effects on response to growth hormone and on risk of sensorineural hearing loss.Semantic proximity Read ↗

Ear and Hearing Problems in Turner's SyndromeSemantic proximity Read ↗

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