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M Y Lan

Showing results (21-30 of 26) with videos related to

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European Journal of Neurology|March 20, 2014
Clinical and genetic analysis of Taiwanese patients with hereditary spastic paraplegia type 5M-Y Lan, T-H Yeh, Y-Y Chang, et al.
Clinical Genetics|April 8, 2010
High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathyM-Y Lan, M-H Fu, Y-F Liu, et al.
Neuroscience Letters|March 14, 2000
Transtentorial cerebellar c-jun expression after focal cerebral cortical injury in miceJ S Liu, Y Y Chang, H S Wu, et al.
Clinical Genetics|May 23, 2018
Mutational analysis of CCM1, CCM2 and CCM3 in a Han Chinese cohort with multiple cerebral cavernous malformations in TaiwanK-Y Jih, C-P Chung, Y-Y Chang, et al.
Allergy|January 26, 2013
Allergic rhinitis and risk of erectile dysfunction--a nationwide population-based studyV Y F Su, C J Liu, M Y Lan, et al.
Annals of Human Genetics|July 17, 2008
HMBS mutations in Chinese patients with acute intermittent porphyriaC-C Yang, H-C Kuo, H-L You, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
European Journal of Neurology|March 20, 2014
Clinical and genetic analysis of Taiwanese patients with hereditary spastic paraplegia type 5M-Y Lan, T-H Yeh, Y-Y Chang, et al.
Clinical Genetics|April 8, 2010
High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathyM-Y Lan, M-H Fu, Y-F Liu, et al.
Neuroscience Letters|March 14, 2000
Transtentorial cerebellar c-jun expression after focal cerebral cortical injury in miceJ S Liu, Y Y Chang, H S Wu, et al.
Clinical Genetics|May 23, 2018
Mutational analysis of CCM1, CCM2 and CCM3 in a Han Chinese cohort with multiple cerebral cavernous malformations in TaiwanK-Y Jih, C-P Chung, Y-Y Chang, et al.
Allergy|January 26, 2013
Allergic rhinitis and risk of erectile dysfunction--a nationwide population-based studyV Y F Su, C J Liu, M Y Lan, et al.
Annals of Human Genetics|July 17, 2008
HMBS mutations in Chinese patients with acute intermittent porphyriaC-C Yang, H-C Kuo, H-L You, et al.
Pageof 3