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

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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:

Scopus:

Білім салалары

Genetics (clinical) Pharmacology (medical)