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Homozygosity for the V37IGJB2mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in Asian populations

机译：纯合子为V37igJB2的纯合理，十五个证据，轻度至中度感觉障碍障碍：进一步确认亚洲群体的致病性和单倍型分析

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Emily Gallant; Lauren Francey; Ellen A. Tsai; Micah Berman; Yaru Zhao; Heather Fetting; Maninder Kaur; Matthew A. Deardorff; Alisha Wilkens; Dinah Clark; Hakon Hakonarson; Heidi L. Rehm; Ian D. Krantz;
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1. Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in Asian populations [J] . GallantE., FranceyL., TsaiE.A., American journal of medical genetics, Part A . 2013,第9期

机译：V37I GJB2突变的纯合性在轻度至中度感音神经性听力障碍的15个先证者中：进一步证实了亚洲人群的致病性和单倍型分析
2. Phonemic restoration by hearing-impaired listeners with mild to moderate sensorineural hearing loss. [J] . Baskent D, Eiler CL, Edwards B Hearing Research: An International Journal . 2010,第1a2期

机译：轻度至中度感音神经性听力损失的听力受损听众的语音恢复。
3. Language Development and Impairment in Children With Mild to Moderate Sensorineural Hearing Loss (vol 60, pg 1551, 2017) [J] . Halliday Lorna F., Tuomainen Outi, Rosen Stuart Journal of speech, language, and hearing research: JSLHR . 2018,第2期

机译：轻度患儿与中度感觉损失的儿童的语言开发和损伤（Vol 60，PG 1551,2017）
4. Auditory selective attention deficits in mild-moderate aphasia: Relation to formally-tested and self-reported auditory comprehension impairments [D] . Asanuma, Natsumi. 2015

机译：轻度-中度失语的听觉选择性注意缺陷：与正式测试和自我报告的听觉理解障碍的关系
5. Homozygosity for the V37I GJB2 Mutation in Fifteen Probands with Mild to Moderate Sensorineural Hearing Impairment: Further Confirmation of Pathogenicity and Haplotype Analysis in Asian Populations [O] . Emily Gallant, Lauren Francey, Ellen A. Tsai, -1

机译：纯合子的V37I GJB2突变在15名轻度至中度感音神经性听力障碍的先证者：亚洲人群的致病性和单倍型分析的进一步确认。
6. Impaired frequency selectivity and sensitivity to temporal fine structure, but not envelope cues, in children with mild-to-moderate sensorineural hearing loss [O] . Lorna F. Halliday, Stuart Rosen, Outi Tuomainen, 2019

机译：频率的选择性受损和敏感性，但不具有轻度至中等感觉损失的儿童的临时精细结构，但不具有包络线索

Homozygosity for the V37IGJB2mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in Asian populations

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