7p22.3 microdeletion: a case study of a patient with congen… — KazNU

7p22.3 microdeletion: a case study of a patient with congenital heart defect, neurodevelopmental delay and epilepsy

2024 · Article

Publication year

2024

Source: Orphanet Journal of Rare Diseases

DOI: 10.1186/s13023-024-03321-8

Scopus: Open in Scopus

Fields of knowledge

Genetics (clinical) Pharmacology (medical)