[BMJ] Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects |
|
This post will be closed automatically in 2026-08-06 09:22
Reward10points
|
| |
post
reply
points
30
10
Non-pharmacological interventions for autism spectrum disorder in children: an overview of systematic reviews
10
Artificial intelligence in cardiovascular imaging: risks, mitigations and the path to safe implementation
10
Effect of maintenance macrolide de-escalation during the Australian summer on exacerbations of obstructive airway diseases: a randomised, double-blind, placebo-controlled trial
10
[Supplementary]Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects
