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1)  Nonsyndromic hearing impairment
非综合征性耳聋
1.
Mutation analysis of GJB2 gene in nonsyndromic hearing impairment patients from Northeastern China;
中国东北地区非综合征性耳聋患者GJB2基因的致聋突变分析
2.
Gene mapping of a nonsyndromic hearing impairment family;
非综合征性耳聋一家系的基因定位
2)  hereditary nonsyndromic deafness
遗传性非综合征性耳聋
3)  nonsyndromic inherited hearing loss
非综合征型遗传性耳聋
4)  non-syndromic hearing loss
遗传性非综合征型耳聋
5)  nonsyndromic hearing loss
非综合征型耳聋
1.
Mutation analysis of12S rRNA andtRNA-Ser ~((UCN)) genes in a large Chinese family with maternally inherited nonsyndromic hearing loss by intermarriage;
近亲结婚所致非综合征型耳聋家系的线粒体基因突变分析
2.
In order to investigate the possible role of mitochondrial DNA mutations in NSHL, we analyze the incidence, character of three types of mitochondrial DNA mutations in the nonsyndromic hearing loss (NSHL) patients and their clinical data, healthy control subjects were also analyzed simultaneously.
分析非综合征型耳聋患者(nonsyndromic hearing loss, NSHL)及健康体检者中3种线粒体DNA(mitochondrial DNA, mtDNA)突变的发生频率、性质及临床资料特点,探讨线粒体DNA突变与非综合征型耳聋的关系。
6)  Non-syndromic deafness
非综合征耳聋
1.
Family of Jiangsu Huaiyin is one of the biggest non-syndromic deafness families in the world.
永久保存珍贵的家系材料,是对该家系进行深入研究的基础,为此采用EB病毒(Epstein Barrvirus,EBV)转化淋巴细胞的方法对中国江苏淮阴地区非综合征耳聋大家系行建系工作。
补充资料:耳聋无闻

耳聋无闻

耳聋无闻   病名。出《灵枢·厥病》。系指完全失去听觉者。多由年高体弱致听力逐渐下降,甚则耳聋无闻,或卒然而致之耳聋。或有出生即耳聋无闻。外伤亦可致耳聋。宜结合全身情况辨证施治之。宜配合针灸治疗。参见耳聋、耳闭、暴聋条。

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