Hanan H Afifi
4PUBLICATIONS
6CO-AUTHORS
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Publications (4)
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|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
|May 17, 2021
Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant.Hanan H Afifi, Ghada Y El-Kamah, Alaa K Kamel
|Apr 09, 2020
Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation.Ghada M H Abdel-Salam, Inas S M Sayed, Hanan H Afifi
|Aug 13, 2019
Lenz-Majewski syndrome in a patient from Egypt.Hanan H Afifi, Mohamed S Abdel-Hamid, Mennat I Mehrez
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