Prenatal diagnosis of cytochrome c oxidase deficiency in cultured amniocytes is hazardous
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference5 articles.
1. Cytochrome c Oxidase Deficiency
2. Two siblings with cytochromec oxidase deficiency
3. The Use of Skin Fibroblast Cultures in the Detection of Respiratory Chain Defects in Patients with Lacticacidemia
4. Assessment of the mitochondrial respiratory chain
5. Mitochondrial DNA mutations and neuromuscular disease
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines;European Journal of Human Genetics;2022-12-13
2. The development of novel quantification assay for mitochondrial DNA heteroplasmy aimed at preimplantation genetic diagnosis of Leigh encephalopathy;Journal of Assisted Reproduction and Genetics;2007-03-08
3. Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variation;Journal of Inherited Metabolic Disease;1999-12
4. Biochemical and molecular investigations in respiratory chain deficiencies;Clinica Chimica Acta;1994-07
5. Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies;The Journal of Pediatrics;1994-02
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3