Mohammad Najajreh

2PUBLICATIONS
2CO-AUTHORS
Respiratory diseasesHaematology
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Publications (2)

|Aug 11, 2026
H Syndrome Associated With Pure Red Cell Aplasia, Rosai-Dorfman Disease, and Sensorineural Hearing Loss: Phenotypic Variability in Three Children With the Same SLC29A3 Mutation.

|Oct 25, 2025
Congenital Anemia Due to Erythropoietin Gene Mutation Presenting With Diamond-Blackfan Anemia-like features.

Ibrahim AboGhayyada, Mohammad Zeidan, Dalya Abusnaina

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Frequent Collaborators

1 joint publications

Hadeel I Bouzia

1 joint publications

Nour H Moosa