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Thrombosis and Haemostasis|December 22, 2010
Identification of three novel plasminogen (PLG) gene mutations in a series of 23 patients with low PLG activityJürgen Klammt, Louise Kobelt, Dilek Aktas, et al.Blood|July 20, 2006
Molecular and clinical spectrum of type I plasminogen deficiency: A series of 50 patientsKatrin Tefs, Maria Gueorguieva, Jürgen Klammt, et al.JAMA|February 23, 2021
Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye, Zheng Li, Zhenxun Wang, et al.Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.Pageof 10