S Z Huang - JoVE Visualize

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Biochemical Medicine and Metabolic Biology|April 1, 1992

Detection of molecular deletions in the Chinese DMD patients using two amplified dystrophin sequencesY T Zeng, M J Chen, Z R Ren, et al.

British Journal of Haematology|October 1, 1987

A new unstable haemoglobin variant: Hb Shanghai [beta 131(H9)Gln----Pro] found in ChinaY T Zeng, Z R Ren, M J Chen, et al.

American Journal of Human Genetics|November 1, 1989

Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase geneT Wang, Y Okano, R Eisensmith, et al.

Science in China. Series B, Chemistry, Life Sciences & Earth Sciences|October 1, 1992

Study of the RNA splicing defect in the common Chinese beta-thalassemia gene, IVS-II nt. 654 C-->T by using mRNA/PCRS Z Huang, Z R Ren, Y T Zeng, et al.

Scientia Sinica. Series B, Chemical, Biological, Agricultural, Medical & Earth Sciences|August 1, 1983

Application of high pressure liquid chromatography and microsequencing methodology in the structural analysis of human hemoglobin variantsY T Zeng, S Z Huang, A Reynolds, et al.

Burns : Journal of the International Society for Burn Injuries|February 1, 1992

Clinical observations and methods for identifying the existence of cultured epidermal allograftsY B Zhao, X F Zhao, A Li, et al.

Blood|December 1, 1985

Hereditary persistence of fetal hemoglobin or (delta beta)o-thalassemia: three types observed in South-Chinese familiesY T Zeng, S Z Huang, B Chen, et al.

American Journal of Human Genetics|March 1, 1991

Identification of a novel phenylketonuria (PKU) mutation in the Chinese: further evidence for multiple origins of PKU in AsiaT Wang, Y Okano, R C Eisensmith, et al.

Hemoglobin|January 1, 1981

Hb Wuming or alpha 2 11(A9)Lys substituting for Gln beta 2Y T Zeng, S Z Huang, L Xu, et al.

Zhonghua Yi Xue Za Zhi|April 21, 2016

[Analysis of large deletion of phenylalanine hydroxylase gene in Chinese patients with phenylketonuria]Y S Yan, F X Yao, S J Hao, et al.

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Showing results (31-40 of 63) with videos related to

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Pageof 7

Biochemical Medicine and Metabolic Biology|April 1, 1992

Detection of molecular deletions in the Chinese DMD patients using two amplified dystrophin sequencesY T Zeng, M J Chen, Z R Ren, et al.

British Journal of Haematology|October 1, 1987

A new unstable haemoglobin variant: Hb Shanghai [beta 131(H9)Gln----Pro] found in ChinaY T Zeng, Z R Ren, M J Chen, et al.

American Journal of Human Genetics|November 1, 1989

Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase geneT Wang, Y Okano, R Eisensmith, et al.

Science in China. Series B, Chemistry, Life Sciences & Earth Sciences|October 1, 1992

Study of the RNA splicing defect in the common Chinese beta-thalassemia gene, IVS-II nt. 654 C-->T by using mRNA/PCRS Z Huang, Z R Ren, Y T Zeng, et al.

Scientia Sinica. Series B, Chemical, Biological, Agricultural, Medical & Earth Sciences|August 1, 1983

Application of high pressure liquid chromatography and microsequencing methodology in the structural analysis of human hemoglobin variantsY T Zeng, S Z Huang, A Reynolds, et al.

Burns : Journal of the International Society for Burn Injuries|February 1, 1992

Clinical observations and methods for identifying the existence of cultured epidermal allograftsY B Zhao, X F Zhao, A Li, et al.

Blood|December 1, 1985

Hereditary persistence of fetal hemoglobin or (delta beta)o-thalassemia: three types observed in South-Chinese familiesY T Zeng, S Z Huang, B Chen, et al.

American Journal of Human Genetics|March 1, 1991

Identification of a novel phenylketonuria (PKU) mutation in the Chinese: further evidence for multiple origins of PKU in AsiaT Wang, Y Okano, R C Eisensmith, et al.

Hemoglobin|January 1, 1981

Hb Wuming or alpha 2 11(A9)Lys substituting for Gln beta 2Y T Zeng, S Z Huang, L Xu, et al.

Zhonghua Yi Xue Za Zhi|April 21, 2016

[Analysis of large deletion of phenylalanine hydroxylase gene in Chinese patients with phenylketonuria]Y S Yan, F X Yao, S J Hao, et al.

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