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Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics
|
December 1, 1990
Monosomy for 21pter-q21: case report and assignment of a DNA clone (Fr8-77) to the deleted segment
K Abe, H X Deng, N Harada, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery
|
February 23, 2022
[Cell heterogeneity of laryngeal carcinoma and evolution trajectory of epithelial cells]
S S Gu, Z S Shen, H X Deng, et al.
Human Molecular Genetics
|
June 1, 1995
The D90A mutation results in a polymorphism of Cu,Zn superoxide dismutase that is prevalent in northern Sweden and Finland
A Själander, G Beckman, H X Deng, et al.
Gene Therapy
|
July 21, 2017
Gene therapy research in Asia
H-X Deng, Y Wang, Q-R Ding, et al.
Annals of Neurology
|
April 1, 1997
Midbrain dopaminergic neuronal degeneration in a transgenic mouse model of familial amyotrophic lateral sclerosis
V Kostic, M E Gurney, H X Deng, et al.
Cytogenetics and Cell Genetics
|
January 1, 1997
Assignment of mitotic arrest deficient protein 2 (MAD2L1) to human chromosome band 5q23.3 by in situ hybridization
L Xu, H X Deng, Y Yang, et al.
Biochemical and Biophysical Research Communications
|
September 28, 2000
Multiple transcripts of the human Cu,Zn superoxide dismutase gene
M Hirano, W Y Hung, N Cole, et al.
American Journal of Medical Genetics
|
July 1, 1991
Penta X syndrome: a case report with review of the literature
R Kassai, I Hamada, H Furuta, et al.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi = Zhonghua Laodong Weisheng Zhiyebing Zazhi = Chinese Journal of Industrial Hygiene and Occupational Diseases
|
October 10, 2019
[Analysis on social security of pneumoconiosis patients in two areas of Chongqing from 2006 to 2018]
H X Deng, X X Wang, C J Qiu, et al.
Human Genetics
|
April 1, 1991
Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs
H X Deng, K Abe, I Kondo, et al.
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Search research articles
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Showing results (11-20 of 61) with videos related to
Sort By:
Page
of 7
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics
|
December 1, 1990
Monosomy for 21pter-q21: case report and assignment of a DNA clone (Fr8-77) to the deleted segment
K Abe, H X Deng, N Harada, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery
|
February 23, 2022
[Cell heterogeneity of laryngeal carcinoma and evolution trajectory of epithelial cells]
S S Gu, Z S Shen, H X Deng, et al.
Human Molecular Genetics
|
June 1, 1995
The D90A mutation results in a polymorphism of Cu,Zn superoxide dismutase that is prevalent in northern Sweden and Finland
A Själander, G Beckman, H X Deng, et al.
Gene Therapy
|
July 21, 2017
Gene therapy research in Asia
H-X Deng, Y Wang, Q-R Ding, et al.
Annals of Neurology
|
April 1, 1997
Midbrain dopaminergic neuronal degeneration in a transgenic mouse model of familial amyotrophic lateral sclerosis
V Kostic, M E Gurney, H X Deng, et al.
Cytogenetics and Cell Genetics
|
January 1, 1997
Assignment of mitotic arrest deficient protein 2 (MAD2L1) to human chromosome band 5q23.3 by in situ hybridization
L Xu, H X Deng, Y Yang, et al.
Biochemical and Biophysical Research Communications
|
September 28, 2000
Multiple transcripts of the human Cu,Zn superoxide dismutase gene
M Hirano, W Y Hung, N Cole, et al.
American Journal of Medical Genetics
|
July 1, 1991
Penta X syndrome: a case report with review of the literature
R Kassai, I Hamada, H Furuta, et al.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi = Zhonghua Laodong Weisheng Zhiyebing Zazhi = Chinese Journal of Industrial Hygiene and Occupational Diseases
|
October 10, 2019
[Analysis on social security of pneumoconiosis patients in two areas of Chongqing from 2006 to 2018]
H X Deng, X X Wang, C J Qiu, et al.
Human Genetics
|
April 1, 1991
Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs
H X Deng, K Abe, I Kondo, et al.
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of 7