Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Erdengqieqieke Ye"'
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
BackgroundPregnancy-related anemia presents a significant health concern for approximately 500 million women of reproductive age worldwide. To better prevent maternal disorders, it is essential to understand the impact of iron deficiency across diffe
Externí odkaz:
https://doaj.org/article/d5d22b93f3194fbea9989e68c15f7b8d
Autor:
Yangying Jia, Jianhai Chen, Jie Zhong, Xuefei He, Li Zeng, Yanmin Wang, Jiakun Li, Shengqian Xia, Erdengqieqieke Ye, Jing Zhao, Bin Ke, Chunyu Li
Publikováno v:
Clinical Genetics. 103:79-86
Hypoplastic left heart syndrome (HLHS) is a rare but fatal birth defect in which the left side of the heart is underdeveloped. HLHS accounts for 2% to 4% of congenital heart anomalies. Whole genome sequencing (WGS) was conducted for a family trio con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8094fa5cbbd5556660fd239b4a655196
https://doi.org/10.1111/cge.14234
https://doi.org/10.1111/cge.14234
Autor:
Rui, Han, Xiaoran, Liu, Erdengqieqieke, Ye, Shuang, Wu, Jing, Zhao, Ling, Duan, Yan, Xia, Jianbing, Ding
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(4)
To analyze the clinical phenotype and genetic basis for a Chinese pedigree suspected for branchiootic syndrome (BOS).The proband was subjected to target-capture high-throughput sequencing to detect potential variant of deafness-associated genes. Cand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c0c6a32f45c3e6833fa64bf18c19a7c
https://pubmed.ncbi.nlm.nih.gov/35446969
https://pubmed.ncbi.nlm.nih.gov/35446969
Autor:
Erdengqieqieke Ye, Rui Han, Yan Xia, Xiaolin La, Zhijuan Liu, Jianbing Ding, Shuang Wu, Ling Duan
Publikováno v:
Medicine
Branchio-Oto (BO) syndrome is one of the common syndromic forms of hearing loss. In this study, we aimed to characterize the clinical and genetic features of BO syndrome in a Chinese deaf family. The proposita in this study was a 29-years-old Chinese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8125a54815a2b0e28e955655696c8b1c
https://doi.org/10.1097/md.0000000000024691
https://doi.org/10.1097/md.0000000000024691
Autor:
Rui Han, Yan Xia, Zhijuan Liu, Shuang Wu, Erdengqieqieke Ye, Ling Duan, Jianbing Ding, Xiaolin La, Han, Rui, Xia, Yan, Liu, Zhijuan, Wu, Shuang, Ye, Erdengqieqieke, Duan, Ling, Ding, Jianbing, La, Xiaolin
Publikováno v:
Medicine; 6/25/2021, Vol. 100 Issue 25, p1-13, 13p