Skip to content
VuFind
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文(繁體)
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
语言
全文检索
题名
作者
主题
索引号
ISBN/ISSN
标签
检索
高级检索
Identification of Novel Recurr...
引用
发送短信
推荐此
打印
导出纪录
导出到 RefWorks
导出到 EndNoteWeb
导出到 EndNote
Permanent link
Identification of Novel Recurrent Copy Number Variations and Regions of Copy-Neutral Loss of Heterozygosity by High Resolution Genomic Array in Pre-Treatment and Relapsed B-CLL.
书目详细资料
Main Authors:
Knight, S
,
Akha, E
,
Timbs, A
,
Enver, T
,
Pettitt, A
,
Taylor, J
,
Hatton, C
,
Schuh, A
格式:
Conference item
出版:
2009
持有资料
实物特征
相似书籍
职员浏览
实物特征
总结:
相似书籍
IDENTIFICATION OF NOVEL RECURRENT COPY NUMBER VARIATIONS BY HIGH RESOLUTION COMPARATIVE GENOME HYBRIDISATION
由: Schuh, A, et al.
出版: (2009)
Quantitative Whole Genome Analysis of Sequential Samples From Patients with B-CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B-Cell Transcription Factors
由: Timbs, A, et al.
出版: (2010)
Quantitative Whole Genome Analysis of Sequential Samples From Patients with B CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B Cell Transcription Factors
由: Timbs, A, et al.
出版: (2010)
Clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL
由: Klintman, J, et al.
出版: (2018)
Integrated analysis of copy number and loss of heterozygosity in primary breast carcinomas using high-density SNP array
由: Ching, H.C., et al.
出版: (2011)