Auditory screening concurrent deafness predisposing genes screening in 10,043 neonates in Gansu province, China.

[1]  Yu Wang,et al.  Screening for delayed-onset hearing loss in preschool children who previously passed the newborn hearing screening. , 2011, International journal of pediatric otorhinolaryngology.

[2]  Lan Lan,et al.  Newborn hearing concurrent gene screening can improve care for hearing loss: a study on 14,913 Chinese newborns. , 2011, International journal of pediatric otorhinolaryngology.

[3]  Qiuju Wang,et al.  Analysis of a large-scale screening of mitochondrial DNA m.1555A>G mutation in 2417 deaf-mute students in northwest of China. , 2010, Genetic testing and molecular biomarkers.

[4]  C. Wei,et al.  High Prevalence of the Connexin 26 (GJB2) Mutation in Chinese Cochlear Implant Recipients , 2009, ORL.

[5]  C. Robertson,et al.  Permanent Bilateral Sensory and Neural Hearing Loss of Children After Neonatal Intensive Care Because of Extreme Prematurity: A Thirty-Year Study , 2009, Pediatrics.

[6]  J. Guan,et al.  GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects , 2008, Acta oto-laryngologica.

[7]  Chuan-Jen Hsu,et al.  Prospective Mutation Screening of Three Common Deafness Genes in a Large Taiwanese Cohort with Idiopathic Bilateral Sensorineural Hearing Impairment Reveals a Difference in the Results between Families from Hospitals and Those from Rehabilitation Facilities , 2007, Audiology and Neurotology.

[8]  L. Lan,et al.  A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China , 2007, Clinical genetics.

[9]  Ronghua Li,et al.  Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation. , 2006, Biochemical and biophysical research communications.

[10]  W. Nance,et al.  Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss. , 2006, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

[11]  H-S Jin,et al.  Genetic basis of hearing loss associated with enlarged vestibular aqueducts in Koreans , 2004, Clinical genetics.

[12]  C. Kennedy,et al.  Universal neonatal hearing screening moving from evidence to practice , 2004, Archives of Disease in Childhood - Fetal and Neonatal Edition.

[13]  D. Harada,et al.  Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese , 2003, European Journal of Human Genetics.

[14]  F. Telischi,et al.  The prevalence of connexin 26 (GJB2) mutations in the Chinese population , 2002, Human Genetics.

[15]  A. Kenneson,et al.  GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: A HuGE review , 2002, Genetics in Medicine.

[16]  C. Morton Genetics, genomics and gene discovery in the auditory system. , 2002, Human molecular genetics.

[17]  A. Summerfield,et al.  Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: questionnaire based ascertainment study. , 2001, BMJ : British Medical Journal.

[18]  V. Sheffield,et al.  Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype–phenotype correlations , 2001, Human mutation.

[19]  A. Parving The need for universal neonatal hearing screening–some aspects of epidemiology and identification , 1999, Acta paediatrica (Oslo, Norway : 1992). Supplement.

[20]  V. Das,et al.  Aetiology of bilateral sensorineural hearing impairment in children: a 10 year study. , 1996, Archives of disease in childhood.

[21]  Gravel Js,et al.  Universal screening for infant hearing impairment. , 1994 .

[22]  K. E. Price Aminoglycoside research 1975-1985: prospects for development of improved agents , 1986, Antimicrobial Agents and Chemotherapy.

[23]  Vickie Thomson,et al.  The Colorado newborn hearing screening project, 1992-1999: on the threshold of effective population-based universal newborn hearing screening. , 2002, Pediatrics.

[24]  X. Estivill,et al.  Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides , 1998 .