Related references
Note: Only part of the references are listed.Analysis of risk factors associated with unilateral hearing loss in children who initially passed newborn hearing screening
Eric N. Appelbaum et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY (2018)
Newborn genetic screening for hearing impairment: a population-based longitudinal study
Chen-Chi Wu et al.
GENETICS IN MEDICINE (2017)
The relationship between the GJB3 c.538C>T variant and hearing phenotype in the Chinese population
Shasha Huang et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY (2017)
Concurrent Genetic and Standard Screening for Hearing Impairment in 9317 Southern Chinese Newborns
Qi Peng et al.
GENETIC TESTING AND MOLECULAR BIOMARKERS (2016)
Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek et al.
NATURE (2016)
PharmGKB summary: very important pharmacogene information for MT-RNR1
Julia M. Barbarino et al.
PHARMACOGENETICS AND GENOMICS (2016)
Cordblood-Based High-Throughput Screening for Deafness Gene of 646 Newborns in Jinan Area of China
Shou-Xia Li et al.
CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY (2015)
American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss
Raye L. Alford et al.
GENETICS IN MEDICINE (2014)
Otoacoustic emissions in newborn hearing screening: A systematic review of the effects of different protocols on test outcomes
Olubunmi V. Akinpelu et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY (2014)
Improved Newborn Hearing Screening Follow-up Results in More Infants Identified
Suhana Alam et al.
JOURNAL OF PUBLIC HEALTH MANAGEMENT AND PRACTICE (2014)
GJB2-associated hearing loss undetected by hearing screening of newborns
Shujiro B. Minami et al.
GENE (2013)
The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss
Luan Linden Phillips et al.
INTERNATIONAL JOURNAL OF AUDIOLOGY (2013)
Newborn hearing concurrent genetic screening for hearing impairment-A clinical practice in 58,397 neonates in Tianjin, China
Junqing Zhang et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY (2013)
Targeted surveillance for postnatal hearing loss: A program evaluation
Rachael Beswick et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY (2012)
Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14,913 Chinese newborns
Qiu-Ju Wang et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY (2011)
Universal newborn hearing screening
H. Patel et al.
PAEDIATRICS & CHILD HEALTH (2011)
Universal newborn hearing screening: Systematic review to update the 2001 US Preventive Services Task Force Recommendation
Heidi D. Nelson et al.
PEDIATRICS (2008)
Year 2007 position statement: Principles and guidelines for early hearing detection and intervention programs
Jackie Busa et al.
PEDIATRICS (2007)
Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness?: Penetrance of GJB2 deafness
Virginia W. Norris et al.
EAR AND HEARING (2006)
Language ability after early detection of permanent childhood hearing impairment
CR Kennedy et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Current concepts: Newborn hearing screening - A silent revolution
CC Morton et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Universal newborn hearing screening - Summary of evidence
DC Thompson et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2001)