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

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

2024 · Article

Жариялану жылы

2024

Дереккөз: Orphanet Journal of Rare Diseases

DOI: 10.1186/s13023-024-03321-8

Scopus: Жазбаны Scopus-та ашу

Білім салалары

Genetics (clinical) Pharmacology (medical)