官方服务：
资源简介：
a proband with Holt-Oram syndrome
应用场景：
创建时间：
2022-04-09
相关数据集
MOESM7 of De novo variants in exomes of congenital heart disease patients identify risk genes and pathways
Additional file 7: Enrichment analysis in CTD and LVO: Table S29. IPA canonical pathways among 59 genes in conotruncal defects (CTD), Table S30. InnateDB pathway analysis among 59 genes in conotruncal
DataCite Commons2024-02-08 更新70
Key regulatory differentially expressed genes in atrial septal defect children treated with occlusion devices
Atrial septal defects (ASDs) is the most common types of cardiac septal defects in congenital heart defects. In addition to traditional therapy, interventional closure has become the main treatment me
NIAID Data Ecosystem30
AVSD trio probands display de novo and inherited variation in genes related to human and mouse cardiac malformations.
AVSD trio probands display de novo and inherited variation in genes related to human and mouse cardiac malformations.
Figshare2016-09-28 更新20
the BSP of DLK1_R .zip
This is the sequencing data about the methylation level of DLK1_R in 25 TOF patients and 5 controls.
DataCite Commons2021-06-10 更新40
Prevalence of congenital heart disease at live birth: an accurate assessment by echocardiographic screening
Prevalence of congenital heart disease at live birth: an accurate assessment by echocardiographic screening
Global Health Data Exchange ()30
