Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Zuojian Yang"'
Publikováno v:
Maternal-Fetal Medicine. 4:245-250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40712df918da6dd8cd620e0a18587449
https://doi.org/10.1097/fm9.0000000000000163
https://doi.org/10.1097/fm9.0000000000000163
Publikováno v:
The journal of obstetrics and gynaecology research. 47(11)
This study aimed to explore the correlation between the ultrasound phenotype and copy number variation (CNV) of abnormal embryos in spontaneous abortion by investigating the abnormal chromosome copy number of embryos at different developmental stages
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::700032d5d19936c5448e52e92ed3aa6a
https://pubmed.ncbi.nlm.nih.gov/34571575
https://pubmed.ncbi.nlm.nih.gov/34571575
Publikováno v:
Journal of Medical Ultrasonics. 46:273-275
Persistent truncus arteriosus (PTA) is a relatively uncommon congenital heart disease, accounting for approximately 0.7-1.4% of all congenital cardiac abnormalities worldwide. PTA is usually accompanied by a single semilunar valve, with leaflets rang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03ddeb77779e01e9601aeac981992394
https://doi.org/10.1007/s10396-018-00926-y
https://doi.org/10.1007/s10396-018-00926-y
Publikováno v:
Journal of Medical Ultrasonics. 44:281-287
To evaluate the accuracy of oblique view extended imaging (OVEI) in locating the position of the fetal conus medullaris. One hundred and twenty-two normal fetuses and five counterparts with spinal bifida received prenatal ultrasound examination. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::386ebd2820075e0151efc442a358f8b0
https://doi.org/10.1007/s10396-017-0773-x
https://doi.org/10.1007/s10396-017-0773-x
Autor:
Yaqin Lei, Zailong Qin, Bobo Xie, Mengting Li, Shiyu Luo, Shang Yi, Jin Wang, Zuojian Yang, Qi Yang, Xin Fan, Hongwei Wei, Jingsi Luo
Publikováno v:
Molecular Medicine Reports.
Hydrocephalus due to aqueductal stenosis (HSAS; Online Mendelian Inheritance in Man #307000) is a rare X‑linked, recessively‑inherited disease characterized by severe hydrocephaly and occasionally adducted thumbs, in addition to intellectual disa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cde48dc82a7299341d9369813bb7e654
https://doi.org/10.3892/mmr.2018.9583
https://doi.org/10.3892/mmr.2018.9583
Autor:
Zuojian Yang, Shui-Hua Yang, Shengli Li, Xue-qin Li, Xiao-xian Tian, Peng-hui Luo, Xin-yan Li
Publikováno v:
Journal of medical ultrasonics (2001). 45(2)
Pulmonary atresia with ventricular septal defect (PA-VSD) is a rare complex congenital heart defect. Major artery-pulmonary collateral arteries (MAPCAs) are characteristic of PA-VSD. Prenatal diagnosis can be achieved in most cases of PA-VSD with rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::126b36b090fbf2b82069e3d47ce03f8a
https://pubmed.ncbi.nlm.nih.gov/28752252
https://pubmed.ncbi.nlm.nih.gov/28752252