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Journal of Child Neurology|September 29, 2011
The natural history of infant spinal muscular atrophy in China: a study of 237 patientsXiushan Ge, Jinli Bai, Yanyu Lu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 31, 2015
[Screening for genetic mutations in hyperphenylalaninemia using Ion Torrent PGM sequencing]Yanyan Cao, Yujin Qu, Fang Song, et al.
Journal of Human Genetics|February 14, 2020
Transmission characteristics of SMN from 227 spinal muscular atrophy core families in ChinaYanyan Cao, Yujin Qu, Jinli Bai, et al.
BMC Musculoskeletal Disorders|August 25, 2021
Bone mineral density and its influencing factors in Chinese children with spinal muscular atrophy types 2 and 3Xiaoyin Peng, Yujin Qu, Xiaohui Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 6, 2008
[In vitro expression and structural analysis of four missense mutations (G247S, E280G, P362T, A434D) of phenylalanine hydroxylase gene]Fang Song, Yujin Qu, Yoshiyuki Okano, et al.
Zhonghua Yi Xue Za Zhi|April 29, 2015
[Analysis of SMN1 gene partial deletion of spinal muscular atrophy based on MLPA]Wenhui Zhang, Yanyan Cao, Fang Song, et al.
Neuromuscular Disorders : NMD|April 11, 2021
Factors associated with delayed diagnosis of spinal muscular atrophy in China and changes in diagnostic delayYanyan Cao, Miaomiao Cheng, Yujin Qu, et al.
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