Associated Papers
Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domain.
Jaradat SA et al.
Molecular Immunology, 2016
Two novel mutations of FBN1 in Jordanian patients with Marfan syndrome.
Jaradat SA et al.
International Journal of Clinical and Experimental Medicine, 2015
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