Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: PEX26[original query] |
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Expanding the clinical and genetic spectrum of Heimler syndrome. Orphanet journal of rare diseases 2019 12 14 (1): 290. Gao Feng-Juan, Hu Fang-Yuan, Xu Ping, Qi Yu-He, Li Jian-Kang, Zhang Yong-Jin, Chen Fang, Chang Qing, Song Fang, Shen Si-Mai, Xu Ge-Zhi, Wu Ji-Ho |
PEX26 gene genotype-phenotype correlation in neonates with Zellweger syndrome. Translational pediatrics 2021 8 10 (7): 1825-1833. He Yue, Lin Sam Bill, Li Wen-Xuan, Yang Lin, Zhang Rong, Chen Chao, Yuan L |
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- Page last updated:Apr 29, 2024
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