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European Journal of Clinical Investigation
|
August 7, 2018
High levels of circulating cell-free DNA are a biomarker of active SLE
Yalan Xu, Yijun Song, Jiazhen Chang, et al.
Journal of Assisted Reproduction and Genetics
|
February 23, 2016
Molecular analysis of DNA in blastocoele fluid using next-generation sequencing
Yixin Zhang, Na Li, Li Wang, et al.
Molecular Genetics & Genomic Medicine
|
September 22, 2020
REDBot: Natural language process methods for clinical copy number variation reporting in prenatal and products of conception diagnosis
Mengmeng Liu, Yunshan Zhong, Hongqian Liu, et al.
The Journal of Molecular Diagnostics : JMD
|
July 8, 2014
Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes
Desheng Liang, Ying Peng, Weigang Lv, et al.
Prenatal Diagnosis
|
February 3, 2017
Contribution of maternal copy number variations to false-positive fetal trisomies detected by noninvasive prenatal testing
Xiya Zhou, Lili Sui, Yalan Xu, et al.
Biology of Reproduction
|
March 21, 2014
Detection of chromosomal aneuploidy in human preimplantation embryos by next-generation sequencing
Li Wang, Xiaohong Wang, Jianguang Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 5, 2019
Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes
Desheng Liang, David S Cram, Hu Tan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 26, 2017
A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations
Mingyu Han, Zhifeng Li, Wenlu Wang, et al.
Clinical Chemistry
|
November 8, 2014
Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART)
Weigang Lv, Xianda Wei, Ruolan Guo, et al.
Chinese Journal of Cancer Research = Chung-Kuo Yen Cheng Yen Chiu
|
July 23, 2020
Low-depth whole genome sequencing reveals copy number variations associated with higher pathologic grading and more aggressive subtypes of lung non-mucinous adenocarcinoma
Zheng Wang, Lin Zhang, Lei He, et al.
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of 8
Search research articles
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Showing results (51-60 of 74) with videos related to
Sort By:
Page
of 8
European Journal of Clinical Investigation
|
August 7, 2018
High levels of circulating cell-free DNA are a biomarker of active SLE
Yalan Xu, Yijun Song, Jiazhen Chang, et al.
Journal of Assisted Reproduction and Genetics
|
February 23, 2016
Molecular analysis of DNA in blastocoele fluid using next-generation sequencing
Yixin Zhang, Na Li, Li Wang, et al.
Molecular Genetics & Genomic Medicine
|
September 22, 2020
REDBot: Natural language process methods for clinical copy number variation reporting in prenatal and products of conception diagnosis
Mengmeng Liu, Yunshan Zhong, Hongqian Liu, et al.
The Journal of Molecular Diagnostics : JMD
|
July 8, 2014
Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes
Desheng Liang, Ying Peng, Weigang Lv, et al.
Prenatal Diagnosis
|
February 3, 2017
Contribution of maternal copy number variations to false-positive fetal trisomies detected by noninvasive prenatal testing
Xiya Zhou, Lili Sui, Yalan Xu, et al.
Biology of Reproduction
|
March 21, 2014
Detection of chromosomal aneuploidy in human preimplantation embryos by next-generation sequencing
Li Wang, Xiaohong Wang, Jianguang Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 5, 2019
Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes
Desheng Liang, David S Cram, Hu Tan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 26, 2017
A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations
Mingyu Han, Zhifeng Li, Wenlu Wang, et al.
Clinical Chemistry
|
November 8, 2014
Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART)
Weigang Lv, Xianda Wei, Ruolan Guo, et al.
Chinese Journal of Cancer Research = Chung-Kuo Yen Cheng Yen Chiu
|
July 23, 2020
Low-depth whole genome sequencing reveals copy number variations associated with higher pathologic grading and more aggressive subtypes of lung non-mucinous adenocarcinoma
Zheng Wang, Lin Zhang, Lei He, et al.
Page
of 8