{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T02:18:54Z","timestamp":1790302734527,"version":"4.1.0"},"reference-count":48,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2023,11,1]],"date-time":"2023-11-01T00:00:00Z","timestamp":1698796800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2023,11,1]],"date-time":"2023-11-01T00:00:00Z","timestamp":1698796800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2023,11,1]],"date-time":"2023-11-01T00:00:00Z","timestamp":1698796800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2023,11,1]],"date-time":"2023-11-01T00:00:00Z","timestamp":1698796800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2023,11,1]],"date-time":"2023-11-01T00:00:00Z","timestamp":1698796800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2023,11,1]],"date-time":"2023-11-01T00:00:00Z","timestamp":1698796800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2023,11,1]],"date-time":"2023-11-01T00:00:00Z","timestamp":1698796800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jpeds.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["The Journal of Pediatrics"],"published-print":{"date-parts":[[2023,11]]},"DOI":"10.1016\/j.jpeds.2023.113620","type":"journal-article","created":{"date-parts":[[2023,7,19]],"date-time":"2023-07-19T02:02:40Z","timestamp":1689732160000},"page":"113620","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":15,"special_numbering":"C","title":["Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic Yield"],"prefix":"10.1016","volume":"262","author":[{"given":"Nobuko","family":"Yamamoto","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jorune","family":"Balciuniene","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tiffiney","family":"Hartman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maria Alejandra","family":"Diaz-Miranda","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emma","family":"Bedoukian","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Batsal","family":"Devkota","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Audrey","family":"Lawrence","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Netta","family":"Golenberg","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maha","family":"Patel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Archana","family":"Tare","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert","family":"Chen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emma","family":"Schindler","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jiwon","family":"Choi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maninder","family":"Kaur","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sarah","family":"Charles","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jiani","family":"Chen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elizabeth A.","family":"Fanning","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elizabeth","family":"Dechene","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kajia","family":"Cao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Murrell R.","family":"Jill","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ramakrishnan","family":"Rajagopalan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yavuz","family":"Bayram","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Matthew C.","family":"Dulik","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John","family":"Germiller","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laura K.","family":"Conlin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ian D.","family":"Krantz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Minjie","family":"Luo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jpeds.2023.113620_bib1","doi-asserted-by":"crossref","first-page":"879","DOI":"10.1016\/S0140-6736(05)71047-3","article-title":"Sensorineural hearing loss in children","volume":"365","author":"Smith","year":"2005","journal-title":"Lancet"},{"key":"10.1016\/j.jpeds.2023.113620_bib2","doi-asserted-by":"crossref","first-page":"2151","DOI":"10.1056\/NEJMra050700","article-title":"Newborn hearing screening--a silent revolution","volume":"354","author":"Morton","year":"2006","journal-title":"N Engl J Med"},{"key":"10.1016\/j.jpeds.2023.113620_bib3","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0219600","article-title":"Prevalence of permanent childhood hearing loss detected at the universal newborn hearing screen: systematic review and meta-analysis","volume":"14","author":"Butcher","year":"2019","journal-title":"PLoS One"},{"key":"10.1016\/j.jpeds.2023.113620_bib4","doi-asserted-by":"crossref","first-page":"486","DOI":"10.1002\/ajmg.1320460504","article-title":"Genetic epidemiological studies of early-onset deafness in the U.S. school-age population","volume":"46","author":"Marazita","year":"1993","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.jpeds.2023.113620_bib5","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1007\/s40136-017-0163-3","article-title":"Diagnosis and treatment of congenital sensorineural hearing loss","volume":"5","author":"Chari","year":"2017","journal-title":"Curr Otorhinolaryngol Rep"},{"key":"10.1016\/j.jpeds.2023.113620_bib6","doi-asserted-by":"crossref","first-page":"975","DOI":"10.1016\/j.otc.2015.07.004","article-title":"Diagnostic evaluation of children with sensorineural hearing loss","volume":"48","author":"Prosser","year":"2015","journal-title":"Otolaryngol Clin North Am"},{"key":"10.1016\/j.jpeds.2023.113620_bib7","doi-asserted-by":"crossref","DOI":"10.1038\/nrdp.2016.94","article-title":"Congenital hearing loss","volume":"3","author":"Korver","year":"2017","journal-title":"Nat Rev Dis Primers"},{"key":"10.1016\/j.jpeds.2023.113620_bib8","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1016\/j.ijporl.2016.09.016","article-title":"International Pediatric Otolaryngology Group (IPOG) consensus recommendations: hearing loss in the pediatric patient","volume":"90","author":"Liming","year":"2016","journal-title":"Int J Pediatr Otorhinolaryngol"},{"key":"10.1016\/j.jpeds.2023.113620_bib9","doi-asserted-by":"crossref","first-page":"R65","DOI":"10.1093\/hmg\/ddz129","article-title":"Gene therapy for hearing loss","volume":"28","author":"Omichi","year":"2019","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.jpeds.2023.113620_bib10","doi-asserted-by":"crossref","DOI":"10.15252\/emmm.202013259","article-title":"Neonatal AAV gene therapy rescues hearing in a mouse model of SYNE4 deafness","volume":"13","author":"Taiber","year":"2021","journal-title":"EMBO Mol Med"},{"key":"10.1016\/j.jpeds.2023.113620_bib11","doi-asserted-by":"crossref","first-page":"4496","DOI":"10.1073\/pnas.1817537116","article-title":"Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model","volume":"116","author":"Akil","year":"2019","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.jpeds.2023.113620_bib12","doi-asserted-by":"crossref","first-page":"441","DOI":"10.1007\/s00439-016-1648-8","article-title":"Comprehensive genetic testing in the clinical evaluation\u00a0of 1119 patients with hearing loss","volume":"135","author":"Sloan-Heggen","year":"2016","journal-title":"Hum Genet"},{"key":"10.1016\/j.jpeds.2023.113620_bib13","doi-asserted-by":"crossref","DOI":"10.1038\/s41598-017-16846-9","article-title":"Combined genetic approaches yield a 48% diagnostic rate in a large\u00a0cohort of French hearing-impaired patients","volume":"7","author":"Baux","year":"2017","journal-title":"Sci Rep"},{"key":"10.1016\/j.jpeds.2023.113620_bib14","doi-asserted-by":"crossref","first-page":"627","DOI":"10.1136\/jmedgenet-2013-101749","article-title":"Advancing genetic testing for deafness with genomic technology","volume":"50","author":"Shearer","year":"2013","journal-title":"J Med Genet"},{"key":"10.1016\/j.jpeds.2023.113620_bib15","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1177\/0194599815591156","article-title":"Massively parallel sequencing for genetic diagnosis of hearing loss: the new standard of care","volume":"153","author":"Shearer","year":"2015","journal-title":"Otolaryngol Head Neck Surg"},{"key":"10.1016\/j.jpeds.2023.113620_bib16","doi-asserted-by":"crossref","first-page":"1600","DOI":"10.1038\/gim.2018.48","article-title":"AUDIOME: a tiered exome sequencing-based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss","volume":"20","author":"Guan","year":"2018","journal-title":"Genet Med"},{"key":"10.1016\/j.jpeds.2023.113620_bib17","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1186\/s13073-020-0712-0","article-title":"A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data","volume":"12","author":"Rajagopalan","year":"2020","journal-title":"Genome Med"},{"key":"10.1016\/j.jpeds.2023.113620_bib18","doi-asserted-by":"crossref","first-page":"705","DOI":"10.1373\/clinchem.2017.280685","article-title":"Allele-specific droplet digital PCR combined with a next-generation sequencing-based algorithm for diagnostic copy number analysis in genes with high homology: proof of concept using stereocilin","volume":"64","author":"Amr","year":"2018","journal-title":"Clin Chem"},{"key":"10.1016\/j.jpeds.2023.113620_bib19","doi-asserted-by":"crossref","first-page":"639","DOI":"10.1016\/j.jmoldx.2014.06.003","article-title":"Comprehensive diagnostic testing for stereocilin: an approach for analyzing medically important genes with high homology","volume":"16","author":"Mandelker","year":"2014","journal-title":"J Mol Diagn"},{"key":"10.1016\/j.jpeds.2023.113620_bib20","doi-asserted-by":"crossref","first-page":"274","DOI":"10.1016\/j.jmoldx.2021.12.002","article-title":"Molecular diagnostic outcomes from 700 cases: what can we learn from a retrospective analysis of clinical exome sequencing?","volume":"24","author":"Murrell","year":"2022","journal-title":"J Mol Diagn"},{"key":"10.1016\/j.jpeds.2023.113620_bib21","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1038\/gim.2015.30","article-title":"Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of medical genetics and genomics and the association for molecular pathology","volume":"17","author":"Richards","year":"2015","journal-title":"Genet Med"},{"key":"10.1016\/j.jpeds.2023.113620_bib22","doi-asserted-by":"crossref","first-page":"1593","DOI":"10.1002\/humu.23630","article-title":"Expert specification of the ACMG\/AMP variant interpretation guidelines for genetic hearing loss","volume":"39","author":"Oza","year":"2018","journal-title":"Hum Mutat"},{"key":"10.1016\/j.jpeds.2023.113620_bib23","doi-asserted-by":"crossref","first-page":"1531","DOI":"10.1002\/humu.24465","article-title":"Long-read sequencing for molecular diagnostics in constitutional genetic disorders","volume":"43","author":"Conlin","year":"2022","journal-title":"Hum Mutat"},{"key":"10.1016\/j.jpeds.2023.113620_bib24","doi-asserted-by":"crossref","first-page":"1837","DOI":"10.1002\/humu.24443","article-title":"Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss","volume":"43","author":"Chen","year":"2022","journal-title":"Hum Mutat"},{"key":"10.1016\/j.jpeds.2023.113620_bib25","doi-asserted-by":"crossref","first-page":"4408","DOI":"10.1038\/s41598-019-40586-7","article-title":"Frequency and clinical features of hearing loss caused by STRC deletions","volume":"9","author":"Yokota","year":"2019","journal-title":"Sci Rep"},{"key":"10.1016\/j.jpeds.2023.113620_bib26","doi-asserted-by":"crossref","first-page":"1673","DOI":"10.1038\/s41436-021-01187-w","article-title":"One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementation","volume":"23","author":"Lincoln","year":"2021","journal-title":"Genet Med"},{"key":"10.1016\/j.jpeds.2023.113620_bib27","doi-asserted-by":"crossref","first-page":"387","DOI":"10.1007\/s00439-021-02365-1","article-title":"Evaluation of copy number variants for genetic hearing loss: a review of current approaches and recent findings","volume":"141","author":"Abbasi","year":"2022","journal-title":"Hum Genet"},{"key":"10.1016\/j.jpeds.2023.113620_bib28","doi-asserted-by":"crossref","first-page":"898","DOI":"10.1542\/peds.2007-2333","article-title":"Year 2007 position statement: principles and guidelines for early hearing detection and intervention programs","volume":"120","author":"Hearing JCoI","year":"2007","journal-title":"Pediatrics"},{"key":"10.1016\/j.jpeds.2023.113620_bib29","doi-asserted-by":"crossref","first-page":"2083","DOI":"10.1007\/s00431-021-03983-7","article-title":"Permanent childhood hearing impairment in infants admitted to the neonatal intensive care unit: nested case-control study","volume":"180","author":"Nair","year":"2021","journal-title":"Eur J Pediatr"},{"key":"10.1016\/j.jpeds.2023.113620_bib30","doi-asserted-by":"crossref","first-page":"972","DOI":"10.1542\/peds.2014-1173","article-title":"Hearing loss and congenital CMV infection: a systematic review","volume":"134","author":"Goderis","year":"2014","journal-title":"Pediatrics"},{"key":"10.1016\/j.jpeds.2023.113620_bib31","doi-asserted-by":"crossref","first-page":"e488","DOI":"10.1097\/MAO.0000000000002234","article-title":"Systematic review of hearing loss genes in the African American population","volume":"40","author":"Worden","year":"2019","journal-title":"Otol Neurotol"},{"key":"10.1016\/j.jpeds.2023.113620_bib32","doi-asserted-by":"crossref","first-page":"611","DOI":"10.1016\/j.ijporl.2010.03.004","article-title":"GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent","volume":"74","author":"Shan","year":"2010","journal-title":"Int J Pediatr Otorhinolaryngol"},{"key":"10.1016\/j.jpeds.2023.113620_bib33","doi-asserted-by":"crossref","first-page":"1012","DOI":"10.1002\/humu.24309","article-title":"Variant interpretation using population databases: lessons from gnomAD","volume":"43","author":"Gudmundsson","year":"2022","journal-title":"Hum Mutat"},{"key":"10.1016\/j.jpeds.2023.113620_bib34","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1007\/s00439-021-02335-7","article-title":"Racial and ethnic disparities in genetic testing for hearing loss: a systematic review and synthesis","volume":"141","author":"Rouse","year":"2022","journal-title":"Hum Genet"},{"key":"10.1016\/j.jpeds.2023.113620_bib35","doi-asserted-by":"crossref","first-page":"114","DOI":"10.1186\/s13023-022-02262-4","article-title":"Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes","volume":"17","author":"Mutai","year":"2022","journal-title":"Orphanet J Rare Dis"},{"key":"10.1016\/j.jpeds.2023.113620_bib36","doi-asserted-by":"crossref","first-page":"1791","DOI":"10.1038\/s41431-019-0471-9","article-title":"A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis","volume":"27","author":"Tan","year":"2019","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.jpeds.2023.113620_bib37","doi-asserted-by":"crossref","first-page":"2211","DOI":"10.1001\/jama.281.23.2211","article-title":"Carrier rates in the midwestern United States for GJB2\u00a0mutations causing inherited deafness","volume":"281","author":"Green","year":"1999","journal-title":"JAMA"},{"key":"10.1016\/j.jpeds.2023.113620_bib38","doi-asserted-by":"crossref","first-page":"411","DOI":"10.1007\/s00439-010-0864-x","article-title":"Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing","volume":"128","author":"Naranjo","year":"2010","journal-title":"Hum Genet"},{"key":"10.1016\/j.jpeds.2023.113620_bib39","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1080\/16513860301713","article-title":"Recommendations for the description of genetic and audiological data for families with nonsyndromic hereditary hearing impairment","volume":"1","author":"Mazzoli","year":"2003","journal-title":"Audiol Med"},{"key":"10.1016\/j.jpeds.2023.113620_bib40","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1186\/s13023-017-0708-z","article-title":"Prevalence of TECTA mutation in patients with mid-frequency\u00a0sensorineural hearing loss","volume":"12","author":"Yamamoto","year":"2017","journal-title":"Orphanet J Rare Dis"},{"key":"10.1016\/j.jpeds.2023.113620_bib41","doi-asserted-by":"crossref","first-page":"1600","DOI":"10.1038\/gim.2018.48","article-title":"AUDIOME: a tiered exome sequencing-based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss","volume":"20","author":"Guan","year":"2018","journal-title":"Genet Med"},{"key":"10.1016\/j.jpeds.2023.113620_bib42","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1186\/s13073-020-0712-0","article-title":"A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data","volume":"12","author":"Rajagopalan","year":"2020","journal-title":"Genome Med"},{"key":"10.1016\/j.jpeds.2023.113620_bib43","doi-asserted-by":"crossref","first-page":"102","DOI":"10.1002\/ajmg.a.20210","article-title":"Use of a multiplex PCR\/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafness","volume":"121a","author":"Wu","year":"2003","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.jpeds.2023.113620_bib44","author":"Van Camp"},{"key":"10.1016\/j.jpeds.2023.113620_bib45","doi-asserted-by":"crossref","first-page":"484","DOI":"10.1016\/j.ajhg.2018.08.006","article-title":"Genomic landscape and mutational signatures\u00a0of\u00a0deafness-associated genes","volume":"103","author":"Azaiez","year":"2018","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.jpeds.2023.113620_bib46","doi-asserted-by":"crossref","first-page":"D1062","DOI":"10.1093\/nar\/gkx1153","article-title":"ClinVar: improving access to variant interpretations and supporting evidence","volume":"46","author":"Landrum","year":"2018","journal-title":"Nucleic Acids Res"},{"key":"10.1016\/j.jpeds.2023.113620_bib47","doi-asserted-by":"crossref","first-page":"434","DOI":"10.1038\/s41586-020-2308-7","article-title":"The mutational constraint spectrum quantified from variation in 141,456 humans","volume":"581","author":"Karczewski","year":"2020","journal-title":"Nature"},{"key":"10.1016\/j.jpeds.2023.113620_bib48","doi-asserted-by":"crossref","first-page":"877","DOI":"10.1016\/j.ajhg.2016.08.016","article-title":"REVEL: an Ensemble method for predicting the pathogenicity of rare missense variants","volume":"99","author":"Ioannidis","year":"2016","journal-title":"Am J Hum Genet"}],"container-title":["The Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022347623004833?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022347623004833?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,20]],"date-time":"2025-09-20T09:19:16Z","timestamp":1758359956000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022347623004833"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,11]]},"references-count":48,"alternative-id":["S0022347623004833"],"URL":"https:\/\/doi.org\/10.1016\/j.jpeds.2023.113620","relation":{},"ISSN":["0022-3476"],"issn-type":[{"value":"0022-3476","type":"print"}],"subject":[],"published":{"date-parts":[[2023,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic Yield","name":"articletitle","label":"Article Title"},{"value":"The Journal of Pediatrics","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jpeds.2023.113620","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2023 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}],"article-number":"113620"}}