Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population
about
Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genes.Gerbode Ventricular Septal Defect -A Rare Cardiac Anomaly Associated with Genetic Variants in Indian Population- A Case Series.The importance of copy number variation in congenital heart diseaseComparison of a teratogenic transcriptome-based predictive test based on human embryonic versus inducible pluripotent stem cells.Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or mult
P2860
Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Genome-wide copy number varian ...... ects in Chinese Han population
@ast
Genome-wide copy number varian ...... ects in Chinese Han population
@en
type
label
Genome-wide copy number varian ...... ects in Chinese Han population
@ast
Genome-wide copy number varian ...... ects in Chinese Han population
@en
prefLabel
Genome-wide copy number varian ...... ects in Chinese Han population
@ast
Genome-wide copy number varian ...... ects in Chinese Han population
@en
P2093
P2860
P1433
P1476
Genome-wide copy number varian ...... ects in Chinese Han population
@en
P2093
Chenxia Nie
Guoying Huang
Hongyan Wang
Wenyuan Duan
Xiaoli Chen
Yiping Shen
P2860
P2888
P356
10.1186/S12920-015-0163-4
P50
P577
2016-01-08T00:00:00Z
P5875
P6179
1017922426