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It's very difficult to treat genetic diseases.

遗传性疾病治疗起来很困难。

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Objective To analyze the clinical feature of children hereditary spherocytosis (HS).

目的分析儿童遗传性球形红细胞增多症的临床特

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We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

遗传性白内障病基因,实验动物模型是一个非常好的方式。

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Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所的一种遗传性代谢疾病。

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In 1990, a family with an inherited speech disorder known as verbal dyspraxia drew the attention of genetics researchers.

1990年,患有遗传性语言障碍(verbaldyspraxia)的一家人引起了基因学者的注意。

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Dyskeratosis congenita (DKC) is a rare inherited disease characterized by the triad of abnormal skin pigmentation, nail dystrophy, and mucosal leukoplakia.

先天性角化不良症(DKC)一少见之遗传性疾病,三项主要特肤色素异常、 指甲生长异常及黏膜白斑症。

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HD is caused by a trinucleotide repeat expansion in the Huntingtin (Htt) gene; and is one of several polyglutamine (or PolyQ) diseases.

什么是'少年亨廷顿疾病-遗传性疾病与异常运动和心理的恶化'?

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In this paper are elaborated the methods of induced obesity by hereditation ,hypothalamic lesions and dietary in experimental animals,and the concerned physiological characteristics.

阐述了遗传性、下丘脑性及饮食诱导性肥胖动物模型的造型方法及有关的生理代谢特.

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This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.

本文报告了一例罕见的遗传性掌跖肤角化病—遗传性残毁性角化瘤,并与各种掌跖肤角化症、断肢症的鉴别进行了讨论。

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Several non-infectious diseases including the leaf red spot, gummosis, herbicide in jury, typhoon damage and genetic albinism and an unidentified leaf crinkle disease are also described.

此外非病原性病害包括红斑病、流胶病、除草剂药害、风害及遗传性白化症等,以及病因不明之尾叶桉皱叶病亦在文内叙述之。

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BBC 听力 2019年5月合集

The treatment is for spinal muscular atrophy, a rare inherited disease that affects infants.

该治方法适用于脊髓肌萎缩症,这是一种影响婴儿的罕见遗传

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双语版 TED-Ed 演讲精选

In hereditary cases, parents pass genetic mutations on to their children.

遗传中,父母将基因突变传递给他们的孩子。

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经济学人(汇总)

In Ghana HI-GENES found one mutation responsible for 40% of inherited deafness.

在加纳,HI-GENES发现了一个导致40%的遗传耳聋的突变。

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日常生活医学科普

Thalassemia is a group of inherited blood disorders.

地中海贫血是一组遗传血液疾

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Osmosis-呼吸

Inheriting CF is more common in people of European descent.

遗传的CF更多见于欧洲人种。

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VOA Special 2023年11月合集

Sickle cell disease (SCD) is a genetic blood disorder that affects millions of people worldwide.

镰状细胞是一种遗传血液疾,影响全球数万人。

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我们这一天 第一季

We learned about inherited traits in science, and rolling your tongue is one.

今天科学课上我们学了遗传状,能卷舌头就是其中之一。

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科学60秒-科学美国人 2022年10月合集

It's one of the most hereditary cancers.

那是遗传最突出的癌症之一。

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美剧疑犯追踪POI第二季

Our friend in Rikers is counting on you.

关在里克岛的那位就指望你了{\an1}{\pos(60,101)}血统:欧洲 身高:183-193厘米 瞳色:蓝色 发色:棕色 需排除的医: 囊纤维化 遗传血色沉着。

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Osmosis-血液肿瘤

Hemophilia usually refers to inherited deficiencies of coagulation factors, which can be either quantitative or qualitative.

血友通常是指遗传的凝血因子缺乏症,可以是数量或者活上的缺陷。

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经济学人-科技

Marriage between cousins is common in Pakistan, and such inbreeding leads to a high incidence of genetic disorders.

近亲结婚在巴基斯坦很普遍,而这种近亲交配引发遗传的发率很高。

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加拿大剧拯救希望第一季

Lynch syndrome. It's also called H.N.P.C.C.

林氏综合症 也叫做遗传非息肉症大肠直肠癌。

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TED演讲(视频版)双语精选

I was born with a genetic condition that affects my mobility and requires me to have assistance.

我先天患有遗传问题,影响了我的行动,需要辅助。

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每日英语听力 | 双语精读

Studies looking for genetic clues have also revealed little, other than the discovery that ADHD is heritable.

寻找遗传线索的研究除了发现ADHD具有遗传外,几乎没有发现其他结果。

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剑桥学霸读书分享

And then the next question would be how do patients with autosomal dominant polycystic kidney disease present?

下一个问题是常染色体显遗传多囊肾患者的表现是怎样的?

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简单心理学

From what researchers can tell, the disorder has a strong genetic component, but also an environmental one.

根据研究,这种疾不仅有很强的遗传,还受环境的影响。

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Osmosis-神经

Alright as a quick recap, spinocerebellar ataxia is a group of progressive neurodegenerative diseases of genetic origin.

得!快速回顾一下~脊髓小脑共济失调是一组遗传进行神经退行

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Vox 观点

It has no bearing on an individual's intelligence… but today it's commonly labeled a hereditary neurobiological learning disability.

这与个人的智力无关。但今天,它通常被称为遗传神经生物学学习障碍。

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双语版 TED-Ed 演讲精选

These genetic changes are estimated to have evolved over the last 3,000 years or so, and are ongoing.

这些遗传变化估计从三千年前开始,并且仍在进化。

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VOA慢速英语_科技

SMA is a genetic disease that slowly destroys motor neurons, nerve cells in the spinal cord that control muscles.

SMA是一种遗传,它会慢慢破坏运动神经元,即脊髓中控制肌肉的神经细胞。

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