听力

Out of the cosmic egg came speech, breath, eyes and sight, ears and hearing, skin, hair, and herbs; from the navel and outbreath came death, and from the organ of pleasure seed and waters were born.

出宇宙蛋来到讲话，呼吸，眼睛和视力，耳朵和听力，皮肤，头发，和草药；从肚脐和outbreath了死刑，并从机关和水域高兴种子出生。

Status quo, factors resulted in hearing im pairment and rehabilitation demands that

求进行深入分析，为国家制定听力残疾的预防及康复策略提供依据。在2780 万

B: Well, my listening isn't too bad, but I still have a lot of problems with s peaking.

是啊，我的听力还可以，但我的口语还有不少问题。

The hearing impairment of the rickety rats is be- lieved to be due mainly to the decrease of the perilymphatic ionized calcium concentration and the impaired blood supply of inner ear caused by rickets.

认为佝偻病引起内耳液钙离子浓度下降和耳蜗供血不足，是导致听力损害的主要原因，佝偻病大白鼠耳蜗对庆大霉素耳毒性有较强的耐受性可能与耳蜗血流量下降有关。

Objective To study the curative effect of ossicular chain reconstruction with postauricular musculo-periosteal-bone flap.

作者：宋忠义王仁祥李建东王烨作者单位：山东省东营市人民医院耳鼻喉科目的探讨用耳后带蒂肌筋膜骨瓣修复听骨链在听力重建手术中的应用。

The degree of hearing loss is moderate to severe, and more pronounced in high frequency. Classically the goiter appears in mid-childhood, but is often postpubertal.

听力损失多为中度至重度，以高频较为严重，甲状腺肿多发生在青春期之后。

The students are all weak in listening, when the teacher prelect in English, many students cannot follow their teacher, and they cannot keep up with their teacher

英语老师自己连这点材料都搞不定？？？1。学生听力普遍较弱，教师用英语讲课时，不少同学听不清、跟不上。

Because Cx43 gene is the first a connexin gene to be associated with non-syndromic deafness, we have sequenced the coding region of Cx43 gene from 190 Taiwanese patients with prelingual deafness and 130 unrelated normal individuals.

Cx43基因是connexin α家族中第一个被发现与非症候群听障有关的基因，我们收集台湾地区190位语言学习前期听障患者，及130位听力正常人血液DNA做Cx43基因的分析。

Methods Forty - six prelingual deaf children and 30 children with normal comprehension were obtained, and the del（ GJB6 - D13S1830） in the Cx30 gene were screened by polymerase chain reaction in 2 groups.

方法收集46例散发的语前聋患儿及听力正常健康对照30例血标本，提取DNA后利用聚合酶链反应分析方法，筛查Cx30基因del（GJB6-D13S1830）突变。

We have sequenced the coding region of Cx26 gene from 190 Taiwanese patients with prelingual deafness and 120 unrelated normal individuals. In the deaf patients, three mutations were found: missense mutation, 551G to A and deletion, 235delC and 299-300delAT.

收集120位听力正常人及190位听障孩童对Cx26基因进行多型性比对发现有5种多型性，其中有4种多型性是之前已被发表的：79G→A(V27I)、109G→A(V37I)、341A→G(E114G)及608T→C(I203T)，另发现有一个新的多型性(558G→A)。

Do you know, i need you to come back

你知道吗，我需要你回来

Yang yinshu、Wang xiangsheng、Li decang,The first discovery of haemaphysalis conicinna.

1〕 杨银书，王祥生，李德昌。安徽省首次发现嗜群血蜱。