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

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

2024 · Article

Год публикации

2024

Источник: Orphanet Journal of Rare Diseases

DOI: 10.1186/s13023-024-03321-8

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Области знаний

Genetics (clinical) Pharmacology (medical)