Cargando…
Analysis of gene copy number variations in patients with congenital heart disease using multiplex ligation-dependent probe amplification
OBJECTIVE: At the molecular and cellular levels, heart development entails the precise orchestration of genetic events such as the interplay of master transcriptional regulators, signaling pathways, and chromatin remodeling. Recent studies among patients with congenital heart disease (CHD) have show...
Autores principales: | Mutlu, Esra Tuba, Hakan Aykan, Hayrettin, Karagöz, Tevfik |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kare Publishing
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237800/ https://www.ncbi.nlm.nih.gov/pubmed/29952356 http://dx.doi.org/10.14744/AnatolJCardiol.2018.70481 |
Ejemplares similares
-
Multiplex Ligation-Dependent Probe Amplification Analysis of GATA4 Gene Copy Number Variations in Patients with Isolated Congenital Heart Disease
por: Guida, Valentina, et al.
Publicado: (2010) -
Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect
por: Zhang, Jingjing, et al.
Publicado: (2015) -
Copy Number Variations and Gene Mutations Identified by Multiplex Ligation-Dependent Probe Amplification in Romanian Chronic Lymphocytic Leukemia Patients
por: Balla, Beata, et al.
Publicado: (2023) -
A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease
por: Zhang, Xiaoqing, et al.
Publicado: (2015) -
Multiplex ligation-dependent probe amplification identifies copy number changes in normal and undetectable karyotype MDS patients
por: Ma, Jing, et al.
Publicado: (2021)