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American Journal of Human Genetics|May 6, 2017
International Cooperation to Enable the Diagnosis of All Rare Genetic DiseasesKym M Boycott, Ana Rath, Jessica X Chong, et al.Journal of the National Cancer Institute|December 24, 2009
Risks of Lynch syndrome cancers for MSH6 mutation carriersLaura Baglietto, Noralane M Lindor, James G Dowty, et al.The Lancet. Rheumatology|January 23, 2024
Lupus low disease activity state and remission and risk of mortality in patients with systemic lupus erythematosus: a prospective, multinational, longitudinal cohort studyRangi Kandane-Rathnayake, Vera Golder, Worawit Louthrenoo, et al.Nature Biotechnology|April 16, 2021
Generation of recombinant hyperimmune globulins from diverse B-cell repertoiresSheila M Keating, Rena A Mizrahi, Matthew S Adams, et al.Advances in Experimental Medicine and Biology|December 8, 2017
Improved Diagnosis and Care for Rare Diseases through Implementation of Precision Public Health FrameworkGareth Baynam, Faye Bowman, Karla Lister, et al.Nature Human Behaviour|October 29, 2021
Global urbanicity is associated with brain and behaviour in young peopleJiayuan Xu, Xiaoxuan Liu, Qiaojun Li, et al.Human Mutation|March 19, 2013
Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domainPartha Sen, Yaping Yang, Colby Navarro, et al.Neuroscience and Biobehavioral Reviews|November 4, 2023
The Human AffectomeDaniela Schiller, Alessandra N C Yu, Nelly Alia-Klein, et al.Pageof 117