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It's very difficult to treat genetic diseases.

疾病治疗起来很困难。

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

目的分析儿童球形红细胞增多症的临床特点。

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

研究内障致病基因,实验动物模型是一个非常好的方式。

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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,患有语言障碍(verbaldyspraxia)的一家人引起了基因学者的注意。

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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.

甲基丙二酸血症是于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种代谢疾病。

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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.

先天角化不良症(DKC)为一少见之疾病,三特徵为皮肤色素异常、 指甲生长异常及黏膜斑症。

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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-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、下丘脑及饮食诱导肥胖动物模型的造型方法及有关的生理代谢特点.

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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掌跖皮肤角化病—残毁角化瘤,并与各种掌跖皮肤角化症、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.

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

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科学60秒-科学美国人 2022年10月合集

It's one of the most hereditary cancers.

那是遗传性癌症

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日常生活医学科普

Thalassemia is a group of inherited blood disorders.

地中海贫血是遗传性血液疾病。

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Osmosis-呼吸

Inheriting CF is more common in people of European descent.

遗传性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.

镰状细胞病是遗传性血液疾病,影响全球数百万人。

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双语版 TED-Ed 演讲精选

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

遗传性病例中,父母将基因传递给他们孩子。

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我们这

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

科学课上我们学了遗传性状,能卷舌头就是其中

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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发现了个导致40%遗传性耳聋

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加拿大剧拯救希望

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

林氏综合症 也叫做遗传性非息肉症大肠直肠癌。

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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.

该治疗方法适用于脊髓性肌萎缩症,这是种影响婴儿罕见遗传性疾病。

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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.

我先患有遗传性问题,影响了我行动,需要辅助。

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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.

这些遗传性化估计从三千年前开始,并且仍在进化。

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

个问题是常染色体显性遗传性多囊肾患者表现是怎样

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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.

血友病通常是指遗传性凝血因子缺乏症,可以是数量或者活性上缺陷。

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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.

寻找遗传线索研究除了发现ADHD具有遗传性外,几乎没有发现其他结果。

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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,这种疾病不仅有很强遗传性,还受环境影响。

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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.

这与个人智力无关。但今,它通常被称为遗传性神经生物学学习障碍。

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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!快速回顾下~脊髓小脑性共济失调是遗传性进行性神经退行性疾病。

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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性疾病发病率很高。

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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是遗传性疾病,它会慢慢破坏运动神经元,即脊髓中控制肌肉神经细胞。

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双语版 TED-Ed 演讲精选

Meanwhile, genetic differences in dopamine, GABA, and endorphin transmission may contribute to risk for developing an alcohol use disorder.

同时,多巴胺、氨基丁酸、内啡肽传导遗传性差异可能会增加酗酒风险。

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