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American Journal of Human Genetics|October 7, 2022
De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movementShenzhao Lu, Mengqi Ma, Xiao Mao, et al.
Medical Image Analysis|June 26, 2026
Beyond the LUMIR challenge: The pathway to foundational registration modelsJunyu Chen, Shuwen Wei, Joel Honkamaa, et al.
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