Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Rungui Xie"'
Publikováno v:
Journal of Pregnancy, Vol 2024 (2024)
Conclusion: Irregular RBC antibody detection is clinically important for both pregnant women with a history of multiple pregnancies and first-time pregnant women. Mur and Dia should be included in the antigenic profile of reagent RBCs that are used f
Externí odkaz:
https://doaj.org/article/ad45a5a1c7614cf88c8ff0501a738b41
Autor:
Kun, Wang, Yanhui, Liu, Baohua, Zhu, Rungui, Xie, Xiaoyan, Zhang, Shundi, Wei, Yi, He, Wanfang, Xu, Yangyang, Lin
Publikováno v:
In Journal of Medical Colleges of PLA April 2012 27(2):71-79
Autor:
Yanhui Liu, Lan Gao, Jiwu Lou, Jian-Xin Liu, Yangyang Lin, Ying Zhao, Yi He, Manna Sun, Wanfang Xu, Rungui Xie
Publikováno v:
Molecular and Cellular Probes. 29:438-441
Objectives The aim of the study was to set up an alternative automatic molecular diagnostic method for deletional α-thalassaemia mutations without gel electrophoresis. Methods Based on the sequence variation within the two Z boxes and melting curve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4e08dc234ddbb956911da4cc9e6411e
https://doi.org/10.1016/j.mcp.2015.07.004
https://doi.org/10.1016/j.mcp.2015.07.004
Autor:
Simin, Wen, Fubing, Wei, Yi, He, Wanfang, Xu, Rungui, Xie, Xiaoyan, Zhang, Yanhui, Liu, Fu, Xiong
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 31(5)
To assess the value of noninvasive fetal trisomy testing based on massively parallel sequencing for the detection of chromosomal deletions and duplications.Peripheral venous blood was taken from pregnant women with a high risk. Free fetal DNA in mate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc40b34afa10edfd4889b991743a4275
https://pubmed.ncbi.nlm.nih.gov/25297580
https://pubmed.ncbi.nlm.nih.gov/25297580
Autor:
Fu Xiong, Yan-hui Liu, Xiao-yan Zhang, Rungui Xie, Yi He, Shun-di Wei, Wang-fang Xu, Yangyang Lin
Publikováno v:
Gene. 509(1)
We describe the prenatal diagnosis and fetal phenotype of partial trisomy 12 (p12-pter) transmitted from a maternal reciprocal translocation 6;12. Genetic analysis was conducted on umbilical cord blood for a fetus accompanied with tricuspid regurgita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3720072c0bb35a083d28c4d6a5a66aa3
https://pubmed.ncbi.nlm.nih.gov/22959136
https://pubmed.ncbi.nlm.nih.gov/22959136