Cargando…
Large-scale copy number variants (CNVs): Distribution in normal subjects and FISH/real-time qPCR analysis
BACKGROUND: Genomic copy number variants (CNVs) involving >1 kb of DNA have recently been found to be widely distributed throughout the human genome. They represent a newly recognized form of DNA variation in normal populations, discovered through screening of the human genome using high-throughp...
Autores principales: | Qiao, Ying, Liu, Xudong, Harvard, Chansonette, Nolin, Sarah L, Brown, W Ted, Koochek, Maryam, Holden, Jeanette JA, Lewis, ME Suzanne, Rajcan-Separovic, Evica |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1920519/ https://www.ncbi.nlm.nih.gov/pubmed/17565693 http://dx.doi.org/10.1186/1471-2164-8-167 |
Ejemplares similares
-
miRNA and miRNA target genes in copy number variations occurring in individuals with intellectual disability
por: Qiao, Ying, et al.
Publicado: (2013) -
Understanding the impact of 1q21.1 copy number variant
por: Harvard, Chansonette, et al.
Publicado: (2011) -
Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID)
por: Qiao, Ying, et al.
Publicado: (2014) -
Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH
por: Tyson, Christine, et al.
Publicado: (2008) -
Functional consequences of copy number variants in miscarriage
por: Wen, Jiadi, et al.
Publicado: (2015)