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M El Khattab

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 7, 2009
A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstreamH Robert-Ebadi, P de Moerloose, M El Khorassani, et al.
Journal of Medical Case Reports|November 15, 2024
Atypical Cogan syndrome: a case reportK El Bouhmadi, A Allaoui, M El Khattab, et al.
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Showing results (1-10 of 2) with videos related to

Sort By:
Pageof 1
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 7, 2009
A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstreamH Robert-Ebadi, P de Moerloose, M El Khorassani, et al.
Journal of Medical Case Reports|November 15, 2024
Atypical Cogan syndrome: a case reportK El Bouhmadi, A Allaoui, M El Khattab, et al.
Pageof 1