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BMC Urology
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December 23, 2014
46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literature
Tian-Fu Li, Qiu-Yue Wu, Cui Zhang, et al.
Journal of Andrology
|
December 18, 2010
Meiotic pairing error in an infertile male bearing reciprocal deletion of chromosome 13
Ying-Xia Cui, Li Wei, Xin-Yi Xia, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 15, 2010
[Mutation analysis of NF2 gene and clinical investigation in a Chinese family with neurofibromatosis type II]
Ying-xia Cui, Xin-yi Xia, Ting-ting Huang, et al.
Molecular Medicine Reports
|
August 12, 2015
A duplication upstream of SOX9 was not positively correlated with the SRY‑negative 46,XX testicular disorder of sex development: A case report and literature review
Xin-Yi Xia, Cui Zhang, Tian-Fu Li, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology
|
September 30, 2010
[Effects of semen analysis on human sperm movement parameters at different times after semen collection]
Yong Shao, Yi-Feng Ge, Xiao-Feng Zhao, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology
|
February 21, 2008
[Semen biochemical markers and their significance in the patients with premature ejaculation]
Bing Yao, Xi-Ying Li, Zhi-Ming Zhao, et al.
American Journal of Medical Genetics. Part A
|
September 19, 2009
A girl with distinctive features of borderline high blood pressure, short stature, characteristic brachydactyly, and 11.47 Mb deletion in 12p11.21-12p12.2 by oligonucleotide array CGH
Hong-Yong Lu, Ying-Xia Cui, Yi-Chao Shi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 22, 2009
A novel insertion mutation in the SEDL gene results in X-linked spondyloepiphyseal dysplasia tarda in a large Chinese pedigree
Xin-Yi Xia, Ying-Xia Cui, Yu-Chun Zhou, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology
|
December 2, 2009
[Evaluation of sperm mitochondrial membrane potential in varicocele patients using JC-1 fluorescent staining]
Yi Hu, Xin-yi Xia, Lian-jun Pan, et al.
Frontiers in Medicine
|
March 27, 2023
A mouse model for X-linked Alport syndrome induced by Del-ATGG in the <i>Col4a5</i> gene
Wei-Qing Wu, Jia-Xun Zhang, Ying-Xia Cui, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 70) with videos related to
Sort By:
Page
of 7
BMC Urology
|
December 23, 2014
46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literature
Tian-Fu Li, Qiu-Yue Wu, Cui Zhang, et al.
Journal of Andrology
|
December 18, 2010
Meiotic pairing error in an infertile male bearing reciprocal deletion of chromosome 13
Ying-Xia Cui, Li Wei, Xin-Yi Xia, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 15, 2010
[Mutation analysis of NF2 gene and clinical investigation in a Chinese family with neurofibromatosis type II]
Ying-xia Cui, Xin-yi Xia, Ting-ting Huang, et al.
Molecular Medicine Reports
|
August 12, 2015
A duplication upstream of SOX9 was not positively correlated with the SRY‑negative 46,XX testicular disorder of sex development: A case report and literature review
Xin-Yi Xia, Cui Zhang, Tian-Fu Li, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology
|
September 30, 2010
[Effects of semen analysis on human sperm movement parameters at different times after semen collection]
Yong Shao, Yi-Feng Ge, Xiao-Feng Zhao, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology
|
February 21, 2008
[Semen biochemical markers and their significance in the patients with premature ejaculation]
Bing Yao, Xi-Ying Li, Zhi-Ming Zhao, et al.
American Journal of Medical Genetics. Part A
|
September 19, 2009
A girl with distinctive features of borderline high blood pressure, short stature, characteristic brachydactyly, and 11.47 Mb deletion in 12p11.21-12p12.2 by oligonucleotide array CGH
Hong-Yong Lu, Ying-Xia Cui, Yi-Chao Shi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 22, 2009
A novel insertion mutation in the SEDL gene results in X-linked spondyloepiphyseal dysplasia tarda in a large Chinese pedigree
Xin-Yi Xia, Ying-Xia Cui, Yu-Chun Zhou, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology
|
December 2, 2009
[Evaluation of sperm mitochondrial membrane potential in varicocele patients using JC-1 fluorescent staining]
Yi Hu, Xin-yi Xia, Lian-jun Pan, et al.
Frontiers in Medicine
|
March 27, 2023
A mouse model for X-linked Alport syndrome induced by Del-ATGG in the <i>Col4a5</i> gene
Wei-Qing Wu, Jia-Xun Zhang, Ying-Xia Cui, et al.
Page
of 7