Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss
Published 2021 View Full Article
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Title
Genetic and Non-genetic Workup for Pediatric Congenital Hearing Loss
Authors
Keywords
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Journal
Frontiers in Pediatrics
Volume 9, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2021-03-22
DOI
10.3389/fped.2021.536730
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Related references
Note: Only part of the references are listed.- ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs
- (2019) Marina T. DiStefano et al. GENETICS IN MEDICINE
- Genetic Testing for Congenital Non-syndromic Sensorineural Hearing Loss
- (2019) Mallory Raymond et al. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
- The etiological evaluation of sensorineural hearing loss in children
- (2019) E. A. van Beeck Calkoen et al. EUROPEAN JOURNAL OF PEDIATRICS
- Advances in Management of Pediatric Sensorineural Hearing Loss
- (2019) C. Carrie Liu et al. OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA
- Utilization of diagnostic testing for pediatric sensorineural hearing loss
- (2018) Carissa J. Wentland et al. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
- An Evidence-Based Practical Approach to Pediatric Otolaryngology in the Developing World
- (2018) Ryan H. Belcher et al. OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA
- The genetic basis of deafness in populations of African descent
- (2017) Jason R. Rudman et al. Journal of Genetics and Genomics
- Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic
- (2016) Devanshi Mehta et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss
- (2016) Christina M. Sloan-Heggen et al. HUMAN GENETICS
- International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient
- (2016) Bryan J. Liming et al. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
- Pediatric otolaryngology, molecular diagnosis of hereditary hearing loss
- (2015) Kayla M. Jasper et al. Current Opinion in Otolaryngology & Head and Neck Surgery
- Clinical application of whole-exome sequencing across clinical indications
- (2015) Kyle Retterer et al. GENETICS IN MEDICINE
- Sensorineural Hearing Loss
- (2015) Asitha D. L. Jayawardena et al. OTOLARYNGOLOGY-HEAD AND NECK SURGERY
- Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss
- (2015) Tahir Atik et al. PLoS One
- American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss
- (2014) GENETICS IN MEDICINE
- Common genes for non-syndromic deafness are uncommon in sub-Saharan Africa: A report from Nigeria
- (2014) Akeem O. Lasisi et al. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
- Diagnostic Yield of MRI for Pediatric Hearing Loss
- (2014) Bart Kachniarz et al. OTOLARYNGOLOGY-HEAD AND NECK SURGERY
- Pediatric Hearing Loss
- (2014) Christopher R. Grindle PEDIATRICS IN REVIEW
- Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment
- (2011) Lauren J. Francey et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A prospective, longitudinal study of the impact ofGJB2/GJB6genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants
- (2009) Christina G.S. Palmer et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
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