找回密码
 To register

QQ登录

只需一步,快速开始

扫一扫,访问微社区

Titlebook: Inheritance of Kidney and Urinary Tract Diseases; Adrian Spitzer,Ellis D. Avner Book 1990 Kluwer Academic Publishers 1990 DNA.diagnosis.ge

[复制链接]
查看: 28967|回复: 54
发表于 2025-3-21 19:11:30 | 显示全部楼层 |阅读模式
书目名称Inheritance of Kidney and Urinary Tract Diseases
编辑Adrian Spitzer,Ellis D. Avner
视频video
丛书名称Topics in Renal Medicine
图书封面Titlebook: Inheritance of Kidney and Urinary Tract Diseases;  Adrian Spitzer,Ellis D. Avner Book 1990 Kluwer Academic Publishers 1990 DNA.diagnosis.ge
描述Genetic disorders have emerged as a prominent cause of morbidity and mor­ tality among infants and adults. As many as 10% to 20% of hospital admis­ sions and at least 10% of the mortality in this age group are due to inherited diseases. There are at least two factors that have brought genetic disorders into the forefront of pediatrics. One is a great reduction in childhood mortality due to infections and nutritional deficiency states, and the other is the rapid progress made in the identification of genetic defects. Amniocentesis, chorionic villus sampling, and recombinant DNA technology have already had a tremendous impact on the practice of medicine. This is why the first two chapters of this volume are dedicated to general principles of molecular genetics and to a description of the techniques used to diagnose genetic disorders at the DNA level. The relevance of this new area of science to the study of inherited renal diseases is reflected in the large body of knowledge that has been generated regarding the association between various glomerular nephritides and genetic markers such as the HLA system, and even more impressively in the direct or indirect identification of abnormal
出版日期Book 1990
关键词DNA; diagnosis; gene; gene expression; genetics; infection; infections; kidney; medicine; membrane; mortality;
版次1
doihttps://doi.org/10.1007/978-1-4613-1603-9
isbn_softcover978-1-4612-8887-9
isbn_ebook978-1-4613-1603-9
copyrightKluwer Academic Publishers 1990
The information of publication is updating

书目名称Inheritance of Kidney and Urinary Tract Diseases影响因子(影响力)




书目名称Inheritance of Kidney and Urinary Tract Diseases影响因子(影响力)学科排名




书目名称Inheritance of Kidney and Urinary Tract Diseases网络公开度




书目名称Inheritance of Kidney and Urinary Tract Diseases网络公开度学科排名




书目名称Inheritance of Kidney and Urinary Tract Diseases被引频次




书目名称Inheritance of Kidney and Urinary Tract Diseases被引频次学科排名




书目名称Inheritance of Kidney and Urinary Tract Diseases年度引用




书目名称Inheritance of Kidney and Urinary Tract Diseases年度引用学科排名




书目名称Inheritance of Kidney and Urinary Tract Diseases读者反馈




书目名称Inheritance of Kidney and Urinary Tract Diseases读者反馈学科排名




单选投票, 共有 1 人参与投票
 

1票 100.00%

Perfect with Aesthetics

 

0票 0.00%

Better Implies Difficulty

 

0票 0.00%

Good and Satisfactory

 

0票 0.00%

Adverse Performance

 

0票 0.00%

Disdainful Garbage

您所在的用户组没有投票权限
发表于 2025-3-21 20:27:06 | 显示全部楼层
978-1-4612-8887-9Kluwer Academic Publishers 1990
发表于 2025-3-22 01:10:54 | 显示全部楼层
发表于 2025-3-22 06:13:41 | 显示全部楼层
发表于 2025-3-22 11:01:26 | 显示全部楼层
发表于 2025-3-22 15:44:25 | 显示全部楼层
Epidemiology of Autosomal Dominant Polycystic Kidney Disease: Implications for Genetic Counselingurrence, but also because of its myriad manifestations. Clinically, ADPKD is characterized by the development of renal cysts and extrarenal manifestations including gastrointestinal, cardiovascular and musculoskeletal abnormalities (Table 12–1).
发表于 2025-3-22 18:15:40 | 显示全部楼层
Genetics of Primary Hyperoxaluria been described, of which type I (glycolic aciduria) is much more common than type II (L-glyceric aciduria) [2]. The discussion will therefore focus on PH type I. Apart from these two types, there appears to exist yet another variety of PH, in which the urinary excretion of both glycolate and glycerate are normal [3–5].
发表于 2025-3-23 00:31:41 | 显示全部楼层
发表于 2025-3-23 05:03:59 | 显示全部楼层
Molecular Biology, Gene Expression, and Medicinet, an explosion in our knowledge about basic cell function. A large number of molecular biology techniques have been standardized [1,2] and even automated [3]; and many of these procedures are rapidly entering diagnostic laboratories.
发表于 2025-3-23 07:32:25 | 显示全部楼层
Approaches to the Diagnosis of Renal Genetic Disorders Using DNA Analysisor alterations from the normal state, in individuals with genetic diseases. Assignment of normal and mutant genes to the human chromosomal map has enabled the diagnosis of genetic diseases, even in cases where the basic biochemical defect underlying the disease in question remains unknown.
 关于派博传思  派博传思旗下网站  友情链接
派博传思介绍 公司地理位置 论文服务流程 影响因子官网 SITEMAP 大讲堂 北京大学 Oxford Uni. Harvard Uni.
发展历史沿革 期刊点评 投稿经验总结 SCIENCEGARD IMPACTFACTOR 派博系数 清华大学 Yale Uni. Stanford Uni.
|Archiver|手机版|小黑屋| 派博传思国际 ( 京公网安备110108008328) GMT+8, 2025-5-18 19:41
Copyright © 2001-2015 派博传思   京公网安备110108008328 版权所有 All rights reserved
快速回复 返回顶部 返回列表