Cargando…
No evidence for copy number and methylation variation in H19 and KCNQ10T1 imprinting control regions in children born small for gestational age
BACKGROUND: There is a substantial genetic component for birthweight variation, and although there are known associations between fetal genotype and birthweight, the role of common epigenetic variation in influencing the risk for small for gestational age (SGA) is unknown. The two imprinting control...
Autores principales: | Murphy, Rinki, Thompson, John MD, Tost, Jörg, Mitchell, Edwin A |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4089969/ https://www.ncbi.nlm.nih.gov/pubmed/24934635 http://dx.doi.org/10.1186/1471-2350-15-67 |
Ejemplares similares
-
Beckwith Wiedemann imprinting defect found in leucocyte but not buccal DNA in a child born small for gestational age
por: Murphy, Rinki, et al.
Publicado: (2012) -
Interpretation challenge of small copy number variations in the imprinting regions
por: Ning, Yi, et al.
Publicado: (2022) -
Copy number variations alter methylation and parallel IGF2 overexpression in adrenal tumors
por: Nielsen, Helene Myrtue, et al.
Publicado: (2015) -
aCNViewer: Comprehensive genome-wide visualization of absolute copy number and copy neutral variations
por: Renault, Victor, et al.
Publicado: (2017) -
Copy number rather than epigenetic alterations are the major dictator of imprinted methylation in tumors
por: Martin-Trujillo, Alex, et al.
Publicado: (2017)