查询词典 deficiency

The text is divided into four parts:Chapter 1 mainly reviews the forepart theories of investors behavior and points out the deficiency and limitation of those theories.

本文共分为四个部分：第一章主要对早期投资者理论进行了回顾，并指出了早期投资者行为理论的不足及缺陷。

The origin of honest deficiency is not the network but the fraudulence in interpersonal communication, and the particularity of network circumstance as an inducing factor.

诚信缺失的根源不在网络，而在于人际交往已有的欺骗性，网络环境的特殊性只是其诱因。

Children sweat more, irritability, night crying, occipital alopecia, ectropion ribs, cranial side, breast, funnel chest symptoms such as a doctor to determine whether the child is an important basis for calcium deficiency.

孩子出汗多、烦躁不安、夜间哭闹、枕部脱发、肋骨外翻、方颅、鸡胸、漏斗胸等症状是医生判断孩子是否缺钙的重要依据。

Children sweat more, irritability, night crying, occipital alopecia, ribs eversion, square skull, chicken, funnel chest symptoms such as a doctor to determine whether the child is an important basis for calcium deficiency.

孩子出汗多、烦躁不安、夜间哭闹、枕部脱发、肋骨外翻、方颅、鸡胸、漏斗胸等症状是医生判断孩子是否缺钙的重要依据。

In severe cases, can cause calcium deficiency rickets, and even give rise to a variety of skeletal deformities, such as the cranial side, table tennis head, bracelet or anklet, ribs eversion, chicken or funnel chest, O-type leg or legs, such as X-type.

宝宝轻度缺钙可表现出以下一些症状，如烦躁、好哭、睡眠不安或易醒、易惊跳、多汗、枕部脱发圈、出牙落后等，缺钙严重者可引起佝偻病，甚至引起各种骨骼畸形，如方颅、乒乓头、手镯或脚镯、肋骨外翻、鸡胸或漏斗胸、O型腿或X型腿等。

An inherited metabolic disorder characterized by the deficiency of an enzyme that is necessary for the metabolism of galactose.

半乳糖症一种遗传的代谢紊乱，因缺乏对半乳糖新陈代谢所必需的酶引起。

The high prevalence of diabetes mellitus type 2 and hypertension in Blacks in the West could be directly related to G6PD deficiency Gaskin R.

糖尿病二型的普及，与西方黑人的

Objective To discuss the relationship between deficiency of microelements and children chronic gastritis.

目的探讨微量元素缺乏与小儿慢性胃炎的关系。

Gaucher disease is an inherited disorder that is caused by a deficiency in an enzyme called glucocerebrosidase.

戈谢病是一种遗传性疾病，是由缺乏一种名为葡萄糖脑苷脂酶的酶引起的。

Recent studies indicate an increased frequency of mutations in the gene encoding glucocerebrosidase, a deficiency of which causes Gaucher's disease, among patients with Parkinson's disease.

最近的研究表明，在帕金森患者的脑苷脂基因编码中突变频率增加。脑苷脂的缺乏可导致高歇氏病。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。