Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Haishen Tian"'
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 38, Iss , Pp 101033- (2024)
Non-immune hydrops fetalis (NIHF) is a common and severe manifestation of many genetic disorders. The ultrasound is an ideal method for diagnosing hydrops fetalis during pregnancy. Since most NIHFs do not have an identifiable cause, determining the u
Externí odkaz:
https://doaj.org/article/a73794be80284e0d87441b5243d61da8
Publikováno v:
Biomolecules, Vol 14, Iss 7, p 826 (2024)
The migration, proliferation, and apoptosis of trophoblastic cells play a crucial role in ensuring the effective preservation of pregnancy at the maternal–fetal interface. Any deviations in the structure and function of these cells might potentiall
Externí odkaz:
https://doaj.org/article/a45a3effe9e1412cb75888366f558ec8
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-6 (2020)
Abstract Background Although Chromosomal microarray analysis (CMA) is a powerful diagnostic technology for detecting chromosomal copy number variants (CNVs), it detects numerous variants of unknown significance (VUSs), which poses a great challenge f
Externí odkaz:
https://doaj.org/article/6e9dbcb576924b30aafd9a6be943d7f3
Publikováno v:
Journal of Genetics. 100
Dandy-Walker malformation (DWM) is characterized by complete or partial agenesis of the cerebellar vermis, cyatic dilatation of the forth ventricle, and enlarged posterior fossa. However, the mechanism is still not completely understood up to now. In
Autor:
Yan Luo, Yanmei Sun, Haishen Tian, Hezhen Lu, Lishuang Ma, Yali Li, Yanshang Zhang, Xiaoping Yu, Jian Gao
BackgroundWith the development of whole-genome sequencing, small chromosomal deletions and duplications could be found by NIPT. This study is to evaluate the clinical significance of fetal chromosomal karyotype analysis and chromosomal microarray ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1445ab151f757856864561d1b8398be4
https://doi.org/10.21203/rs.3.rs-74234/v1
https://doi.org/10.21203/rs.3.rs-74234/v1
Autor:
Pingping, Zhang, Yanmei, Sun, Haishen, Tian, Limin, Rong, Fangna, Wang, Xiaoping, Yu, Yali, Li, Jian, Gao
Publikováno v:
Journal of genetics. 99
Smith-Magenis syndrome (SMS, OMIM: 182290) is a multiple congenital anomalies and intellectual disability syndrome due to a 3.45 Mb microdeletion involving 17p11.2 and is estimated to occur about one in 25,000 births. Up to now, the ultrasound findin
Publikováno v:
Journal of Genetics; 2021, Vol. 100 Issue 2, p1-4, 4p, 1 Black and White Photograph
Autor:
Yan LUO, Bingyi ZHAO, Yanmei SUN, Haishen TIAN, Yali LI, Yanshang ZHANG, Jian GAO, Zhiqiang CUI
Publikováno v:
Zhongguo quanke yixue, Vol 25, Iss 20, Pp 2482-2488 (2022)
Background Noninvasive prenatal screening is more effective in screening for fetal aneuploidy than does traditional serological screening. We attempted to analyze the real-world data about the positive predictive value (PPV) for chromosome aneuploidy
Externí odkaz:
https://doaj.org/article/061b7e51135e42428b7b937d01bbb1bf