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World Journal of Pediatrics : WJP|October 23, 2013
Isolated persistent elevation of alanine transaminase for early diagnosis of pre-symptomatic Wilson's disease in Chinese childrenJoannie Hui, Yuet-Ping Yuen, Chung-Mo Chow, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 27, 2004
Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activityAngel On-Kei Chan, Ching-Wan Lam, Sui-Fan Tong, et al.
Cancer Genetics|June 12, 2012
Multiple CDK/CYCLIND genes are amplified in medulloblastoma and supratentorial primitive neuroectodermal brain tumorMeihua Li, Will Lockwood, Maria Zielenska, et al.
Neurology. Genetics|April 12, 2016
Expanding genotype/phenotype of neuromuscular diseases by comprehensive target capture/NGSXia Tian, Wen-Chen Liang, Yanming Feng, et al.
Journal of Nephrology|September 15, 2004
Novel mutations of the AGXT gene causing primary hyperoxaluria type 1Yuet-Ping Yuen, Chi-Kong Lai, Gensy Mei-Wah Tong, et al.
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