Last Posted: Sep 01, 2017
- Information About Early Hearing Detection and Intervention (EHDI) State Programs
- CDC Grand Rounds: Newborn Screening for Hearing Loss and Critical Congenital Heart Disease
MMWR Weekly / August 25, 2017 / 66(33);888?890 - Predictive Value of GJB2 Mutation Status for Hearing Outcomes of Pediatric Cochlear Implantation.
Abdurehim Yasin et al. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2017 Jul 157(1) 16-24 - Outcome of Cochlear Implantation in Prelingually Deafened Children According to Molecular Genetic Etiology.
Park Joo Hyun et al. Ear and hearing 38(5) e316-e324 - Congenital hearing loss.
Korver Anna M H et al. Nature reviews. Disease primers 2017 01 16094 - Molecular diagnostics for hereditary hearing loss in children.
Sommen Manou et al. Expert review of molecular diagnostics 2017 Aug (8) 751-760 - CDC Grand Rounds: Newborn Screening for Hearing Loss and Critical Congenital Heart Disease
MMWR Weekly / August 25, 2017 / 66(33);888?890 - Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss.
Chen Ying et al. Prenatal diagnosis 2016 Dec 36(13) 1233-1241 - Expanded Newborn Screening: Information and Resources for the Family Physician.
Weismiller David Glenn et al. American family physician 2017 Jun 95(11) 703-709 - It’s Loud Out There: Hearing Health across the Lifespan
CDC Public Health Grand Rounds, June 20, 2017 - Advances in genetic hearing loss: CIB2 gene.
Jacoszek Agnieszka et al. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2016 Oct - Navigating genetic diagnostics in patients with hearing loss.
Sloan-Heggen Christina M et al. Current opinion in pediatrics 2016 Dec (6) 705-712 - Too Loud! For Too Long! Loud noises damage hearing
CDC Vital Signs, February 2017 - The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands.
Zazo Seco Celia et al. European journal of human genetics : EJHG 2016 Dec - Application of SNPscan in Genetic Screening for Common Hearing Loss Genes.
Gao Zixuan et al. PloS one 2016 11(10) e0165650 - International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient.
Liming Bryan J et al. International journal of pediatric otorhinolaryngology 2016 Nov 90251-258
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