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

Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project

23 Jan 2020

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 BRCA gene mutations in cancer
Share to Genomics and Rare Diseases
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 31974413
DOI: 10.1038/s41436-019-0745-1

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

Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing projectPMID 31974413Read ↗

Unraveling the genetic basis of post-infancy diagnosed sensorineural hearing loss using whole exome sequencing.Semantic proximity Read ↗

Methods and feasibility study for exome sequencing as a universal second-tier test in newborn screeningSemantic proximity Read ↗

Whole-exome sequencing and its impact in hereditary hearing loss.Semantic proximity Read ↗

Implementing next-generation sequencing for diagnosis and management of hereditary hearing impairment: a comprehensive review.Semantic proximity Read ↗

Using the phenome and genome to improve genetic diagnosis for deafness.Semantic proximity Read ↗

Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approachSemantic proximity Read ↗

Genetic screening of newborns for deafness over 11 years in Beijing, China: More infants could benefit from an expanded program.Semantic proximity Read ↗

Newborn genetic screening for hearing impairment: a population-based longitudinal study.Semantic proximity Read ↗

Comprehensive genotype-phenotype correlation analysis in 11 509 neonates carrying common deafness-associated pathogenic variants.Semantic proximity Read ↗

Next generation sequencing as a follow-up test in an expanded newborn screening programmeSemantic proximity Read ↗

Whole Genome Sequencing and Newborn ScreeningSemantic proximity Read ↗

Next-generation sequencing for genetic testing of hearing loss populations.Semantic proximity Read ↗

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