It's very difficult to treat genetic diseases.
性疾
治疗起来很困难。
It's very difficult to treat genetic diseases.
性疾
治疗起来很困难。
Objective To analyze the clinical feature of children hereditary spherocytosis (HS).
目的分析儿童性球形红细胞
的临床特点。
We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.
研究性白内障致
基因,实验动物模型是一个非常好的方式。
In 1990, a family with an inherited speech disorder known as verbal dyspraxia drew the attention of genetics researchers.
1990年,患有性语言障碍(verbaldyspraxia)的一家人引起了基因学者的注意。
Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.
甲基丙二酸血是由于甲基丙二酰辅
A变位
或其辅
腺苷钴胺素缺陷所致的一种
性代谢疾
。
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(DKC)为一少见之
性疾
,三项主要特徵为皮肤色素异常、 指甲生长异常及黏膜白斑
。
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-
性疾
与异常运动和心理的恶化'?
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点.
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性掌跖皮肤角化
—
性残毁性角化瘤,并与各种掌跖皮肤角化
、断肢
的鉴别进行了讨论。
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.
此外非原性
害包括红斑
、流胶
、除草剂药害、风害及
性白化
等,以及
因不明之尾叶桉皱叶
亦在文内叙述之。
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