Amal M Mohamed
3PUBLICATIONS
2CO-AUTHORS
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Publications (3)
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|Nov 27, 2025
Deciphering copy number variations and gene implications in an Egyptian cohort with autism spectrum disorders.Amal M Mohamed, Ola M Eid, Khalda S Amr
|Jul 29, 2025
Molecular characterization of imprinting disorders: Beckwith-Wiedemann, Silver-Russell, and Prader-Willi syndromes in Egyptian patients.Amal M Mohamed, Ola Eid, Marwa Farid
|Oct 05, 2021
Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.Amal M Mohamed, Alaa K Kamel, Maha M Eid
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