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Xue-Fan Gu

Showing results (11-20 of 71) with videos related to

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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 5, 2007
[A novel mutation of the alpha-L-iduronidase gene in a patient with mucopolysaccharidosis type I]Wei Dou, Chao Peng, Jun-ke Zheng, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|June 5, 2002
[Expression of green fluorescent protein vector by promoter sequence of CYP21 gene and CYP21P gene]Bei Han, Xiu-Min Wang, Ya-Fen Zhang, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|September 27, 2014
The oxidative molecular regulation mechanism of NOX in children with phenylketonuriaYing-Zhong He, Xue-Fan Gu, Li-Hua Lu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|September 7, 2004
[Molecular genetic analysis of congenital lipoid adrenal hyperplasia]Wen-Juan Qiu, Jun Ye, Bei Han, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 12, 2004
[Study on mutations of exon 12 of the PAH gene in 127 phenylketonuria patients]Wen-juan Qiu, Ya-fen Zhang, Jun Ye, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 1, 2005
[Screening and diagnosis of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency with tetrahydrobiopterin loading test]Zhi-xin Zhang, Jun Ye, Wen-juan Qiu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 1, 2005
[Application of tandem mass spectrometry in diagnosis of organic acidemias]Lian-shu Han, Xiao-lan Gao, Jun Ye, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 9, 2005
[Tetrahydrobiopterin loading test in differential diagnosis among hyperphenylalaninemia patients]Zhi-xin Zhang, Jun Ye, Wen-juan Qiu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|February 6, 2014
[Analysis of clinical manifestations and genetic mutations in a child with Laron syndrome]Guo-ying Chang, Shao-ke Chen, Xue-fan Gu, et al.
World Journal of Pediatrics : WJP|January 20, 2017
Eight novel MUT loss-of-function missense mutations in Chinese patients with isolated methylmalonic academiaLian-Shu Han, Zhuo Huang, Feng Han, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 5, 2007
[A novel mutation of the alpha-L-iduronidase gene in a patient with mucopolysaccharidosis type I]Wei Dou, Chao Peng, Jun-ke Zheng, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|June 5, 2002
[Expression of green fluorescent protein vector by promoter sequence of CYP21 gene and CYP21P gene]Bei Han, Xiu-Min Wang, Ya-Fen Zhang, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|September 27, 2014
The oxidative molecular regulation mechanism of NOX in children with phenylketonuriaYing-Zhong He, Xue-Fan Gu, Li-Hua Lu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|September 7, 2004
[Molecular genetic analysis of congenital lipoid adrenal hyperplasia]Wen-Juan Qiu, Jun Ye, Bei Han, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 12, 2004
[Study on mutations of exon 12 of the PAH gene in 127 phenylketonuria patients]Wen-juan Qiu, Ya-fen Zhang, Jun Ye, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 1, 2005
[Screening and diagnosis of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency with tetrahydrobiopterin loading test]Zhi-xin Zhang, Jun Ye, Wen-juan Qiu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 1, 2005
[Application of tandem mass spectrometry in diagnosis of organic acidemias]Lian-shu Han, Xiao-lan Gao, Jun Ye, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 9, 2005
[Tetrahydrobiopterin loading test in differential diagnosis among hyperphenylalaninemia patients]Zhi-xin Zhang, Jun Ye, Wen-juan Qiu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|February 6, 2014
[Analysis of clinical manifestations and genetic mutations in a child with Laron syndrome]Guo-ying Chang, Shao-ke Chen, Xue-fan Gu, et al.
World Journal of Pediatrics : WJP|January 20, 2017
Eight novel MUT loss-of-function missense mutations in Chinese patients with isolated methylmalonic academiaLian-Shu Han, Zhuo Huang, Feng Han, et al.
Pageof 8