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Clinical Laboratory
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September 8, 2017
A Novel Case of 15q24 Microdeletion Syndrome Detected by MLPA in a Chinese Family
Xiao-Ying Dai, Lu Zhou, Yang Liu, et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University
|
May 23, 2008
[Effect of neoadjuvant chemotherapy on ERCC1 gene expression in breast cancer]
Jian-Min Fu, Jie Zhou, Jian-Sheng Xie, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics
|
October 19, 2016
[Gene mutation analysis and prenatal diagnosis of four pedigrees with methymalonic aciduria]
Yu-Chun Pan, Yang Liu, Wei-Qing Wu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
November 19, 2011
[Mutation of thyroid peroxidase gene in 35 patients with congenital hypothyroidism]
Hai-fei Li, Yi-xin Liu, Jian-sheng Xie, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics
|
March 18, 2017
[Two novel TSC2 frameshift mutations in tuberous sclerosis complex]
Yu-Chun Pan, Wei-Qing Wu, Jian-Sheng Xie, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics
|
December 24, 2015
[Genetic and prenatal diagnosis for four families with Williams-Beuren syndrome]
Yang Liu, Zhi-Yong Xu, Wei-Qing Wu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
February 6, 2014
[One case of 2q37 deletion syndrome: clinical and genetic diagnosis]
Qian Geng, Jian-sheng Xie, Wei-qing Wu, et al.
Reproductive Biomedicine Online
|
November 1, 2011
Identification of novel missense mutations of the TGFBR3 gene in Chinese women with premature ovarian failure
Chun-rong Qin, Shi-ling Chen, Ji-long Yao, et al.
Reproductive Biology and Endocrinology : RB&E
|
December 20, 2011
FOXE1 polyalanine tract length screening by MLPA in idiopathic premature ovarian failure
Chun-rong Qin, Ji-long Yao, Wen-jie Zhu, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology
|
December 13, 2021
[46,XY DSD induced by a novel mutation c.458T>C (p.Leu153Pro) of the LHCGR gene: A case report and review of the literature]
Zhi-Yong Xu, Jia-Xun Zhang, Yang Liu, et al.
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Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Clinical Laboratory
|
September 8, 2017
A Novel Case of 15q24 Microdeletion Syndrome Detected by MLPA in a Chinese Family
Xiao-Ying Dai, Lu Zhou, Yang Liu, et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University
|
May 23, 2008
[Effect of neoadjuvant chemotherapy on ERCC1 gene expression in breast cancer]
Jian-Min Fu, Jie Zhou, Jian-Sheng Xie, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics
|
October 19, 2016
[Gene mutation analysis and prenatal diagnosis of four pedigrees with methymalonic aciduria]
Yu-Chun Pan, Yang Liu, Wei-Qing Wu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
November 19, 2011
[Mutation of thyroid peroxidase gene in 35 patients with congenital hypothyroidism]
Hai-fei Li, Yi-xin Liu, Jian-sheng Xie, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics
|
March 18, 2017
[Two novel TSC2 frameshift mutations in tuberous sclerosis complex]
Yu-Chun Pan, Wei-Qing Wu, Jian-Sheng Xie, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics
|
December 24, 2015
[Genetic and prenatal diagnosis for four families with Williams-Beuren syndrome]
Yang Liu, Zhi-Yong Xu, Wei-Qing Wu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
February 6, 2014
[One case of 2q37 deletion syndrome: clinical and genetic diagnosis]
Qian Geng, Jian-sheng Xie, Wei-qing Wu, et al.
Reproductive Biomedicine Online
|
November 1, 2011
Identification of novel missense mutations of the TGFBR3 gene in Chinese women with premature ovarian failure
Chun-rong Qin, Shi-ling Chen, Ji-long Yao, et al.
Reproductive Biology and Endocrinology : RB&E
|
December 20, 2011
FOXE1 polyalanine tract length screening by MLPA in idiopathic premature ovarian failure
Chun-rong Qin, Ji-long Yao, Wen-jie Zhu, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology
|
December 13, 2021
[46,XY DSD induced by a novel mutation c.458T>C (p.Leu153Pro) of the LHCGR gene: A case report and review of the literature]
Zhi-Yong Xu, Jia-Xun Zhang, Yang Liu, et al.
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of 3