Research Articles
Decoding a Genetic Mystery: How Mouse Models Are Revealing the Secrets of Cornelia de Lange Syndrome
Explore how Nipbl-mutant mouse models are providing crucial insights into Cornelia de Lange Syndrome, a rare genetic disorder affecting multiple body systems.
A Fishy Clue to a Human Mystery: Unlocking Cornelia de Lange Syndrome
Discover how zebrafish models are revolutionizing our understanding of Cornelia de Lange Syndrome, a rare genetic disorder affecting development.
The Silent Symphony of Genes: Unraveling Cornelia de Lange Syndrome Through a Chinese Case Study
A comprehensive analysis of Cornelia de Lange Syndrome through a Chinese case study with SMC3 mutation, exploring genetic mechanisms and clinical implications.