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Radiomics analysis of placenta on T2WI facilitates prediction of postpartum haemorrhage: A multicentre study 期刊论文
EBIOMEDICINE, 2019, 卷号: 50, 页码: 355-365
作者:  Wu, Qingxia;  Yao, Kuan;  Liu, Zhenyu;  Li, Longfei;  Zhao, Xin
收藏  |  浏览/下载：126/0  |  提交时间：2020/03/30
Whole-Exome Sequencing Identified a Novel Compound Heterozygous Genotype in ASL in a Chinese Han Patient with Argininosuccinate Lyase Deficiency 期刊论文
BIOMED RESEARCH INTERNATIONAL, 2019, 页码: 7
作者:  Zhao, Mei;  Hou, Lingling;  Teng, Huajing;  Li, Jinchen;  Wang, Jiesi
收藏  |  浏览/下载：59/0  |  提交时间：2019/06/12
Enrichment and Identification of Fetal Nucleated Red Blood Cells from Maternal Blood with Magnetic Nanoparticles and Quantum Dots 期刊论文
NANOSCIENCE AND NANOTECHNOLOGY LETTERS, 2019, 卷号: 11, 期号: 1
作者:  Hou, Xiuwei;  Du, Zhenwu;  Yang, Qiwei;  Yang, Wensheng;  Song, Yang
收藏  |  浏览/下载：25/0  |  提交时间：2019/12/05
Isolation and characterization of a novel benzophenone-3-degrading bacterium Methylophilus sp. strain FP-6. 期刊论文
Ecotoxicology and environmental safety, 2019, 卷号: Vol.186, 页码: 109780
作者:  Chao Jin;  Zhenlong Geng;  Xintong Pang;  Yue Zhang;  Gang Wang
收藏  |  浏览/下载：19/0  |  提交时间：2019/11/21
Psychological factors influencing choice of prenatal diagnosis in Chinese multiparous women with advanced maternal age 期刊论文
JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2019, 卷号: 32, 期号: 14
作者:  Cheng, Bi-Heng;  Chen, Jian-Hua;  Wang, Gao-Hua
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/05
Clinical application of chromosomal microarray analysis for the diagnosis of Williams–Beuren syndrome in Chinese Han patients 期刊论文
Molecular Genetics & Genomic Medicine, 2019, 卷号: Vol.7 No.2
作者:  Yu Xia;  Shufang Huang;  Yueheng Wu;  Yongchao Yang;  Shaoxian Chen
收藏  |  浏览/下载：24/0  |  提交时间：2019/12/13
Genetic diagnosis and prenatal diagnosis of autosomal dominant polycystic kidney disease 期刊论文
2019, 卷号: 36, 期号: 5, 页码: 419-423
作者:  Biyuan Q.[1,2];  Jiyun Y.[3,4,5]
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/16
Accurate diagnosis of fetal cleft lip/palate by typical signs of magnetic resonance imaging 期刊论文
Prenatal Diagnosis, 2019
作者:  Tian M.;  Xiao L.;  Jian N.;  Wei X.;  Liu S.
收藏  |  浏览/下载：8/0  |  提交时间：2019/12/11
Novel loss‑of‑function mutation in BRCA2 gene identified in a Chinese female with a family history of ovarian cancer: A case report 期刊论文
Oncology Letters, 2019, 卷号: Vol.17 No.3, 页码: 3350-3354
作者:  Yanzhi Cui;  Yanyan Wang;  Ningzhi Zhang;  Jun He;  Hui Huang
收藏  |  浏览/下载：23/0  |  提交时间：2019/12/17
Clinical diagnosis and genetic counseling of atypical ataxia‑telangiectasia in a Chinese family. 期刊论文
Molecular medicine reports, 2019
作者:  Jiangxia Cao;  Ruiqin Shen;  Wenqian Zhang;  Bing Mao;  Qirong Shi
收藏  |  浏览/下载：18/0  |  提交时间：2019/12/17

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