7p22.3 microdeletion: a case study of a patient with congen鈥arabi University

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

2024 路 Article
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Publication year

2024

Authors

Source: Orphanet Journal of Rare Diseases

DOI:

Scopus:

Fields of knowledge

Genetics (clinical) Pharmacology (medical)