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Cytogenetic and Genome Research
|
July 14, 2020
Comparative Functional Analysis in vitro of 2 COL4A5 Splicing Mutations at the Same Site in 2 Unrelated Alport Syndrome Chinese Families
Xing Lv, Wei-Qing Wu, Jia-Xun Zhang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 30, 2008
A novel RNA-splicing mutation in COL1A1 gene causing osteogenesis imperfecta type I in a Chinese family
Xin-Yi Xia, Ying-Xia Cui, Yu-Feng Huang, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology
|
February 21, 2008
[Clinical, molecular and cytogenetic studies on 4 patients with 46, XX (SRY positive) male syndrome]
Xin-Yi Xia, Ying-Xia Cui, Hong-Yong Lu, et al.
Journal of Andrology
|
July 21, 2009
A case of agonadism associated with y-chromosome rearrangement: cytogenetic and molecular studies
Ying-Xia Cui, Yi-Chao Shi, Qi Liu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 15, 2010
Association between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men
Yi-chao Shi, Li Wei, Ying-xia Cui, et al.
Molecular Medicine Reports
|
March 12, 2015
A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): a case report
Yu-Chun Zhou, Cui Zhang, Jin-Sheng Zhai, et al.
Cytogenetic and Genome Research
|
May 10, 2018
The COL4A3 and COL4A4 Digenic Mutations in cis Result in Benign Familial Hematuria in a Large Chinese Family
Ang Li, Ying-Xia Cui, Xing Lv, et al.
Cytogenetic and Genome Research
|
April 19, 2018
Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes
Ang Li, Er-Zhi Gao, Ying-Xia Cui, et al.
Plos One
|
November 14, 2013
Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria
Ying-Xia Cui, Xin-Yi Xia, Yang Zhou, et al.
Plos One
|
May 26, 2017
Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome
Jian-Hong Liu, Xiu-Xiu Wei, Ang Li, et al.
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Showing results (61-70 of 70) with videos related to
Sort By:
Page
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This site can display upto 70 results.
Cytogenetic and Genome Research
|
July 14, 2020
Comparative Functional Analysis in vitro of 2 COL4A5 Splicing Mutations at the Same Site in 2 Unrelated Alport Syndrome Chinese Families
Xing Lv, Wei-Qing Wu, Jia-Xun Zhang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 30, 2008
A novel RNA-splicing mutation in COL1A1 gene causing osteogenesis imperfecta type I in a Chinese family
Xin-Yi Xia, Ying-Xia Cui, Yu-Feng Huang, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology
|
February 21, 2008
[Clinical, molecular and cytogenetic studies on 4 patients with 46, XX (SRY positive) male syndrome]
Xin-Yi Xia, Ying-Xia Cui, Hong-Yong Lu, et al.
Journal of Andrology
|
July 21, 2009
A case of agonadism associated with y-chromosome rearrangement: cytogenetic and molecular studies
Ying-Xia Cui, Yi-Chao Shi, Qi Liu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 15, 2010
Association between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men
Yi-chao Shi, Li Wei, Ying-xia Cui, et al.
Molecular Medicine Reports
|
March 12, 2015
A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): a case report
Yu-Chun Zhou, Cui Zhang, Jin-Sheng Zhai, et al.
Cytogenetic and Genome Research
|
May 10, 2018
The COL4A3 and COL4A4 Digenic Mutations in cis Result in Benign Familial Hematuria in a Large Chinese Family
Ang Li, Ying-Xia Cui, Xing Lv, et al.
Cytogenetic and Genome Research
|
April 19, 2018
Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes
Ang Li, Er-Zhi Gao, Ying-Xia Cui, et al.
Plos One
|
November 14, 2013
Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria
Ying-Xia Cui, Xin-Yi Xia, Yang Zhou, et al.
Plos One
|
May 26, 2017
Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome
Jian-Hong Liu, Xiu-Xiu Wei, Ang Li, et al.
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of 7