A new study published in Science Advances sheds light on how changes in brain connections before and after puberty might explain why some children with a rare genetic condition called 22q11.2 deletion ...

22q11.2 Deletion Syndrome (22q11.2 DS) is the most common chromosomal microdeletion disorder, arising chiefly from de novo non-homologous meiotic recombination events. This condition presents with a ...