Investigation of 22q11.2 Deletion Syndrome in the first Moroccan Pediatric Patients series
Tunis Med. 2025 Feb 5;103(2):276-283. doi: 10.62438/tunismed.v103i2.5080. ABSTRACT INTRODUCTION: The 22q11.2 deletion syndrome (22q11DS) is an autosomal dominant genetic syndrome, frequently due to a microdeletion …