Analyzing the journey of discovering ascorbic acid,to make a theory on the genetic defect of the mankind about ascorbic acid.
通过对维生素C发现历程的分析,提出并阐述了人类抗坏血酸遗传缺陷学说。
Some genetic defects could result in phenotype changes and impact pig industry.
猪的遗传缺陷是由于猪生殖细胞或受精卵中的遗传物质在结构或功能上发生了改变,从而使发育的个体表现出的缺陷或异常。
"Severe combined immunodeficiency (SCID), which arises from several different genetic defects, disrupts all of these."
严重复合免疫不全症是由几个不同的遗传缺陷造成,因而全面瓦解。
"More than 60% are caused by an inherited defect in the fetus, which might result in a fatal abnormality."
60%以上的自然流产是因为胎儿有遗传缺陷,可能会造成致命的畸形。
In such cases, the condition can mistakenly be thought to skip generations.
以下就是一个简短的说明对于遗传缺陷是如何被继承和表达的。
That is, if only one parent is affected, the condition will show up in each successive generation.
遗传缺陷可能会出现在任何犬种和犬只集体内的任何系统上。
Polymorphism of Major Genes of Three Genetic Defects in Seven Native Pig Breeds of Guizhou Province
七种贵州地方猪品种的三种遗传缺陷主效基因多态性研究
Detection of an inherited defect:von Willebrand Disease by PCR-RFLP in five police dog breeds
利用PCR-RFLP检测五大不同品种警犬遗传缺陷—血管性假性血友病
For example, one article claimed that we might clone humans to select out genetic defects or select for desirable traits.
比如，有一篇文章声称我们可以通过克隆人去除遗传缺陷或者选择所希望的特性。
Genotyping using comparative DNA analysis to determine the predisposition of individuals to certain diseases was then performed.
然后用比较DNA分析的方法做基因分型来判定个体对某种疾病的遗传缺陷。
The Formation and Heredity of Defects from PAN Precursor to Carbon Fiber
PAN原丝至碳纤维缺陷的形成与遗传性
Study on Clinical and Pathologic Mechanism of Hereditary Antithrombin Deficiency;
遗传性抗凝血酶缺陷症的临床与发病机理研究
"Gene-protein" Theory of Intelligence Disable Hereditary Illness and Gene Remedy;
智力缺陷遗传病的“基因—蛋白质”机制与基因治疗
Nursing Care of Continuous Renal Replacement Therapy in the Treatment of Hereditary Metabolic Disease with Acute Organic Acidosis
CRRT治疗遗传性代谢缺陷病合并重症有机酸血症的护理
Prenatal diagnosisó refers to diagnosis of the fetus regarding its congenital defect and hereditary diseases.
产前诊断，是指对胎儿进行先天性缺陷和遗传性疾病的诊断。
The Study on Phenotype and Genotype of Protein C in a Family with Hereditary Protein C Deficiency;
一个遗传性蛋白C缺陷家系蛋白C表型和基因型研究
Identification of a Novel Deletion Mutation of F13A Gene in a Pedigree with Factor XIII Deficiency;
一种新的凝血因子XIII基因突变导致的遗传性FXIII缺陷症
Genetic Disorders of Cholesterol Biosynthesis-Pathophysiological Studies of Smith-Lemli-Opitz Syndrome;
遗传性胆固醇合成缺陷性疾病的病理生理研究—史—伦—奥三氏综合征
Preclinical Research of Inherited Anti-coagulation Factor and Acquired Coagulation Factor Deficiency;
遗传性抗凝因子和获得性凝血因子缺陷症的基础研究
Pro 275 Ser Homozygous Mutation of PROC Gene Causes Type Ⅱ Inherited Protein C Deficiency
Pro 275 Ser纯合突变导致的Ⅱ型遗传性蛋白C缺陷症