Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Cheng-Zeng Wang"'
Autor:
Yun-Yun Qin, Taibing Fan, Lin Liu, Cunying Cui, Hongdan Wang, Cheng-Zeng Wang, Bangtian Peng, Lianzhong Zhang
Publikováno v:
Oncotarget
// Lin Liu 1, * , Hong-Dan Wang 2, * , Cun-Ying Cui 1 , Yun-Yun Qin 1 , Tai-Bing Fan 3 , Bang-Tian Peng 3 , Lian-Zhong Zhang 1 and Cheng-Zeng Wang 4 1 Department of Cardiovascular Ultrasound, Henan Provincial People’s Hospital, Zhengzhou University
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::069e599b0e961afd3a5ffffd484a2e88
https://doi.org/10.18632/oncotarget.22202
https://doi.org/10.18632/oncotarget.22202
Publikováno v:
Journal of Ultrasound in Medicine. 33:2125-2129
OBJECTIVES To explore the application of instantaneous wave intensity for early diagnosis of systemic lupus erythematosus (SLE)-induced atherosclerosis, we observed carotid elasticity by instantaneous wave intensity in premenopausal women with SLE. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c082b61a366e3c5ae3db731160cf9c9
https://doi.org/10.7863/ultra.33.12.2125
https://doi.org/10.7863/ultra.33.12.2125
Publikováno v:
The Journal of Gene Medicine
Background Little information is available regarding the penetrance of 1q21.1 copy number variants (CNVs). In the present study, we explored the clinical significance of 1q21.1 microdeletion or microduplication. Methods In four families, chromosome k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d37cf09a26504bf561cc789d44bd31
https://doi.org/10.1002/jgm.2948
https://doi.org/10.1002/jgm.2948
Autor:
Cun-Ying Cui, Taibing Fan, Lin Liu, Bangtian Peng, Lian-zhong Zhang, Tao Li, Cheng-Zeng Wang, Dong Wu, Hongdan Wang
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
To explore the underlying pathogenesis and provide references for genetic counseling and prenatal gene diagnosis, we analyzed the chromosome karyotypes and genome-wide copy number variations
To explore the underlying pathogenesis and provide references for genetic counseling and prenatal gene diagnosis, we analyzed the chromosome karyotypes and genome-wide copy number variations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::590a48ee8b7213d3640a8acf3e54ec27
https://doi.org/10.1097/md.0000000000005552
https://doi.org/10.1097/md.0000000000005552
Autor:
Lin Liu, Hong-Dan Wang, Cun-Ying Cui, Dong Wu, Tao Li, Tai-Bing Fan, Bang-Tian Peng, Lian-Zhong Zhang, Cheng-Zeng Wang, Liu, Lin, Wang, Hong-Dan, Cui, Cun-Ying, Wu, Dong, Li, Tao, Fan, Tai-Bing, Peng, Bang-Tian, Zhang, Lian-Zhong, Wang, Cheng-Zeng
Publikováno v:
Medicine; 12/6/2016, Vol. 95 Issue 49, p1-11, 11p