copy number variants 读音:美英 copy number variants基本解释 拷贝数变异;变异 分词解释 copy复制品 number数 variants变体( variant的名词复数 ) copy number variants是什么意思 copy number variants怎么读 copy number variants在线翻译 copy number variants中文意思 copy number variants的解释 copy number variants...
blog.sina.com.cn|基于11个网页 2. 拷贝数量变异 这些"拷贝数量变异(copy number variants)" 的影响已经在高淀粉类饮食(high-starch diets)的族群中获得证实,他们比那 … only-perception.blogspot.com|基于2个网页 3. 拷贝数多态性 拷贝数多态性(copy number variants)常用实验方法介绍分享: 分享到新浪Qing 喜...
Using this method, copy number changes at a level of 5–10 kilobases of DNA sequences can be detected. 使用这种方法,可以检测到5-10kb水平的拷贝数变化。 LASER-wikipedia2 Around 5% of cases of schizophrenia are understood to be at least partially attributable to rare copy number variants (...
In the last years, in particular, new developments in genome-wide scanning methodologies have enabled the association of anumber of previously uncharacterized copy number variants (CNVs, gain or loss of DNA) in AD. Because of the exceedingly large number of studies performed, it has become ...
Abbreviations NDD: Neurodevelopmental disorders; ASD: Autism spectrum disorders; ID: Intellectual disability; iPSCs: Induced pluripotent stem cells; SNVs: Single nucleotide variants; CNVs: Copy number variants; WBS: Williams-Beuren syndrome; PMDS: Phelan-McDermid syndrome; miRNA: MicroRNA; lncRNA: ...
Copy number variants (CNVs) have become increasingly instrumental in understanding the etiology of all diseases and phenotypes, including Neurocognitive Disorders (NDs). Among the well-established regions associated with ND are small parts of chromosome 16 deletions (16p11.2) and chromosome 15 duplication...
Copy number variation and schizophrenia. Over the last 12 months, a series of major articles have reported associations with schizophrenia of copy number variants at 1q21, 15q11.2, 15q13.3, 16p11... David,S Clair - 《Schizophrenia Bulletin》 被引量: 104发表: 2009年 MAGI1 Copy Number Variat...
DNA copy number variants (CNVs) are found in 15% of subjects with ID but their association with phenotypic abnormalities has been predominantly studied in smaller cohorts of subjects with detailed yet non-systematically categorized phenotypes, or larger cohorts (thousands of cases) with smaller number...
Known risk loci for endometrial cancer explain approximately one third of familial endometrial cancer. However, the association of germline copy number var
Part of the missing heritability may be caused by copy number variants (CNVs). In a dataset of children recruited for a history of reading disability (RD, also known as dyslexia) or attention deficit hyperactivity disorder (ADHD) and their siblings, we investigated the effects of CNVs on ...