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European Journal of Human Genetics : EJHG|October 23, 2003
Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2Sixto Garcia-Miñaur, Lampros A Mavrogiannis, Sahan V Rannan-Eliya, et al.American Journal of Human Genetics|August 1, 1997
Evidence for a familial pregnancy-induced hypertension locus in the eNOS-gene regionR Arngrímsson, C Hayward, S Nadaud, et al.Allergy|January 26, 2017
Programmed cell death-1 expression correlates with disease severity and IL-5 in chronic rhinosinusitis with nasal polypsI Kortekaas Krohn, S Bobic, J Dooley, et al.Scientific Reports|October 21, 2017
Evidence for long-term sensitization of the bowel in patients with post-infectious-IBSD Balemans, S U Mondelaers, V Cibert-Goton, et al.Nature Communications|July 6, 2021
Monocyte-driven atypical cytokine storm and aberrant neutrophil activation as key mediators of COVID-19 disease severityL Vanderbeke, P Van Mol, Y Van Herck, et al.Pageof 8