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

Sharing GJB2/GJB6 genetic test information with family members.

Journal of genetic counseling - 1 Jun 2007

Blase Terri, Martinez Ariadna, Grody Wayne W, Schimmenti Lisa, Palmer Christina G S

Abstract excerpt

Although GJB2/GJB6 genetic testing for non-syndromic hearing loss is available, there is no information regarding sharing of test results with family members. A qualitative study was conducted to elucidate if, how, and why parents of a child with hearing loss share GJB2/GJB6 test results with relatives. Parents whose child had testing (n = 7 positive, n = 4 negative, n = 1 inconclusive results) participated in a...

Read the complete abstract on PubMed

Topics

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

Share to Adaptation, Psychological
Share to Connexin 26
Share to Connexin 30

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexins

Share to Genetic Counseling

Share to Health Knowledge, Attitudes, Practice

Share to Hearing Loss, Sensorineural

Share to Privacy

Source

Identifiers

PMID: 17318457
DOI: 10.1007/s10897-006-9066-z

Genes

GJB2
GJB6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Sharing GJB2/GJB6 genetic test information with family members.PMID 17318457Read ↗

The Qualitative Experiences of Otolaryngologists with Genetic Services in the Evaluation of Pediatric Hearing LossSemantic proximity Read ↗

Parent experiences with genetic testing for pediatric hearing lossSemantic proximity Read ↗

Survey On Disclosing Information To Children With Genetic Conditions And Their Siblings In JapanSemantic proximity Read ↗

"My Plate is Full": Reasons for Declining a Genetic Evaluation of Hearing Loss.Semantic proximity Read ↗

Communicating inherited genetic risk between parent and child: a meta-thematic synthesis.Semantic proximity Read ↗

"It's good to know": experiences of gene identification and result disclosure in familial epilepsies.Semantic proximity Read ↗

Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child.Semantic proximity Read ↗

Impact of gene patents and licensing practices on access to genetic testing for hearing loss.Semantic proximity Read ↗

Sharing Genetic Test Results in Lynch Syndrome: Communication With Close and Distant RelativesSemantic proximity Read ↗

Prelingual siblings of children with GJB2 hearing loss: issues to consider.Semantic proximity Read ↗

Pediatric otolaryngologists' use of genetic testing.Semantic proximity Read ↗

What is in a cause? Exploring the relationship between genetic cause and felt stigma.Semantic proximity Read ↗

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