Hilden / Fong / Shenzhen / San Diego / St. Louis / /
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Shearer AE / Google / Gene Codes Corporation / Qiagen / HP / Creative Commons / BioMed Central Ltd. / Stephens / B. / /
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Germany / Mongolia / United States / China / / /
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National Human Genome Research Institute / Stephens K. University of Washington / Nationalities University / Inner Mongolia University / Affiliated Hospital of Inner Mongolia University / University School / /
IndustryTerm
study protocol / online submission / /
MedicalCondition
severe hearing impairment / C1509G human hearing loss / moderate hearing impairment / Hereditary hearing loss homepage / dominant nonsyndromic hearing loss Background Hearing loss / Human nonsyndromic sensorineural deafness / nonsyndromic autosomal dominant hearing loss / TB / different deafness / human autosomal dominant nonsyndromic deafness / display hearing loss / zona pellucida domain / autosomal recessive hearing loss / Korean deafness / Audiometric evaluation Sanger sequencing Hearing impairment / congenital hearing loss / nonsyndromic hearing loss / deafness / profound hearing impairment / autosomal dominant non-syndromic hearing impairment / common sensory disorders / MS / hearing loss / hearing impairment / TECTA-based human hereditary deafness / mid-frequency hearing loss / unilateral otosclerosis / mid-frequency hearing impairment / mild hearing impairment / visual dysfunction / zona pellucida domain protein secretion / disease / hereditary hearing loss overview / zona / hereditary hearing loss / dominant nonsyndromic hearing loss / autosomal dominant non-syndromic hearing loss / autosomal dominant nonsyndromic hearing loss / diabetes mellitus / DFNB21 hearing loss / progressive / mid frequency hearing loss / autosomal dominant hearing loss / /
MedicalTreatment
surgery / /
Organization
National Human Genome Research Institute / Inner Mongolia University / National Natural Science Foundation of China / Committee on Clinical Investigation / Washington University School of Medicine / Nationalities University / Affiliated Hospital / Inner Mongolia University for the Nationalities / General Services Administration / University of Washington / Seattle / /
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Sanger / Van Laer / Van de Heyning / Van Hauwe / Neck Surg / /
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candidate for human autosomal dominant nonsyndromic deafness / contributions HB / author / Adam MP / Workman / representative / Head / /
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php / /
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Washington / Missouri / Massachusetts / Guangdong / /
Technology
alpha / Genomics / study protocol / Human Genome / http / genotype / /
The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro