Hisham Megahed
3PUBLICATIONS
17CO-AUTHORS
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Publications (3)
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|Mar 25, 2021
Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders.Romain Duval, Gaël Nicolas, Alexandra Willemetz
|Nov 20, 2020
Clinical and genetic characterization of ten Egyptian patients with Wolf-Hirschhorn syndrome and review of literature.Mona K Mekkawy, Alaa K Kamel, Manal M Thomas
|Jul 18, 2018
Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration.Ashleigh E Schaffer, Martin W Breuss, Ahmet Okay Caglayan
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Frequent Collaborators
1 joint publications
Ashleigh E Schaffer
1 joint publications
Jamel Chelly
1 joint publications
Joseph G Gleeson
1 joint publications
Engy A Ashaat
1 joint publications
Heba ElAwady
1 joint publications
Romain Duval
1 joint publications
Gaël Nicolas
1 joint publications
Bérengere Koehl
1 joint publications
Marie Hully
1 joint publications
Karine Siquier
