X F Gu - JoVE Visualize

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Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|January 15, 2003

[Studies on chemical constituents from Euphorbia fischeriana Steud]W Z Liu, F L He, Z Y Ruan, et al.

Human Genetics|January 1, 1994

Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresisX F Gu, F de Rooij, G Voortman, et al.

Genetics and Molecular Research : GMR|March 3, 2015

Microsatellite marker analysis reveals the distinction between the north and south groups of hard clam (Meretrix meretrix) in ChinaX F Gu, Y H Dong, H H Yao, et al.

Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1993

[Expression of cyclin B in megakaryocytes and cells of other hematopoietic lines]X F Gu, A Allain, L Li, et al.

Human Genetics|March 1, 1993

High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyriaX F Gu, F de Rooij, J S Lee, et al.

Animal : an International Journal of Animal Bioscience|March 27, 2012

Microarray analysis of genes differentially expressed in the liver of lean and fat chickensH B Wang, Q G Wang, X Y Zhang, et al.

Clinical Chemistry|January 1, 1992

Denaturing gradient gel electrophoresis for rapid detection of latent carriers of a subtype of acute intermittent porphyria with normal erythrocyte porphobilinogen deaminase activityF Bourgeois, X F Gu, J C Deybach, et al.

Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 14, 2023

[Clinical characteristics of 111 cases with mucopolysaccharidosis ⅣA]M N Yi, H W Zhang, X L Gao, et al.

Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 4, 2016

[Blood 7-ketocholesterol level, clinical features and gene mutation analysis of 18 children with Niemann-Pick disease type C]X Zhan, N Lin, H W Zhang, et al.

Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 11, 2018

[Clinical, molecular genetic analysis, and treatment of 3 children with sitosterolemia]D Fang, L L Liang, W J Qiu, et al.

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Showing results (31-40 of 59) with videos related to

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Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|January 15, 2003

[Studies on chemical constituents from Euphorbia fischeriana Steud]W Z Liu, F L He, Z Y Ruan, et al.

Human Genetics|January 1, 1994

Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresisX F Gu, F de Rooij, G Voortman, et al.

Genetics and Molecular Research : GMR|March 3, 2015

Microsatellite marker analysis reveals the distinction between the north and south groups of hard clam (Meretrix meretrix) in ChinaX F Gu, Y H Dong, H H Yao, et al.

Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1993

[Expression of cyclin B in megakaryocytes and cells of other hematopoietic lines]X F Gu, A Allain, L Li, et al.

Human Genetics|March 1, 1993

High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyriaX F Gu, F de Rooij, J S Lee, et al.

Animal : an International Journal of Animal Bioscience|March 27, 2012

Microarray analysis of genes differentially expressed in the liver of lean and fat chickensH B Wang, Q G Wang, X Y Zhang, et al.

Clinical Chemistry|January 1, 1992

Denaturing gradient gel electrophoresis for rapid detection of latent carriers of a subtype of acute intermittent porphyria with normal erythrocyte porphobilinogen deaminase activityF Bourgeois, X F Gu, J C Deybach, et al.

Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 14, 2023

[Clinical characteristics of 111 cases with mucopolysaccharidosis ⅣA]M N Yi, H W Zhang, X L Gao, et al.

Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 4, 2016

[Blood 7-ketocholesterol level, clinical features and gene mutation analysis of 18 children with Niemann-Pick disease type C]X Zhan, N Lin, H W Zhang, et al.

Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 11, 2018

[Clinical, molecular genetic analysis, and treatment of 3 children with sitosterolemia]D Fang, L L Liang, W J Qiu, et al.

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