Author

Amir Abadi

Institution: An-Najah National University

Observed institution: An-Najah National University

ORCID: 0009-0002-6303-7460

Observed ORCID: 0009-0002-6303-7460

OpenAlex ID: A5144250528

Infantile 22q11.2 deletion syndrome with secondary monogenic variants following inconclusive whole exome sequencing: a case report

2026 · Amir Abadi, Usra I. Ghanem, et al. · Frontiers in Pediatrics

Asphyxiating thoracic dystrophy associated with IFT74 pathogenic variant: a case report

2026 · Amir Abadi, Banan Ateeq, et al. · BMC Pediatrics

A Junctional Epidermolysis Bullosa Patient (COL17A1 Gene) With Diabetes Mellitus Type 1: A Rare Case Report

2026 · Amir Abadi, Usra Ghanem, et al. · Case Reports in Dermatological Medicine

Works count: 3

Citation count:

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