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浏览/检索结果: 共11条，第1-10条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes 期刊论文 Genetics in Medicine, 2019 作者:  Desheng Liang;  David S. Cram;  Hu Tan;  Siyuan Linpeng;  Yingdi Liu 收藏  |  浏览/下载：105/0  |  提交时间：2019/12/13 22q11.2 microdeletions  copy-number variation (CNV)  microdeletion/microduplication syndromes (MMS)  noninvasive prenatal screening  positive predictive value (PPV)   Isobaric tag for relative and absolute quantitation based quantitative proteomics reveals unique urinary protein profiles in patients with preeclampsia 期刊论文 2019, 卷号: 23, 期号: 8, 页码: 5822-5826 作者:  Ding, Wenyan;  Qiu, Bintao;  Cram, David S.;  Chen, Xiuting;  Li, Shengjie 收藏  |  浏览/下载：60/0  |  提交时间：2020/01/03 differential expression  GO pathways  iTRAQ  KEGG pathways  PE  proteomics  urine   Preferential selection and transfer of euploid noncarrier embryos in preimplantation genetic diagnosis cycles for reciprocal translocations 期刊论文 FERTILITY AND STERILITY, 2017, 卷号: 108, 期号: 4 作者:  Wang, Li;  Shen, Jiandong;  Cram, David S.;  Ma, Minyue;  Wang, Hui 收藏  |  浏览/下载：33/0  |  提交时间：2019/12/04 Balanced/euploid embryos  mate pair sequencing  preimplantation genetic diagnosis  reciprocal translocations  translocation breakpoints   Placental Up-Regulation of Leptin and ARMS2 is Associated with Growth Discordance in Monochorionic Diamniotic Twin Pregnancies 期刊论文 TWIN RESEARCH AND HUMAN GENETICS, 2017, 卷号: 20, 期号: 2 作者:  Zhang, Jianguang;  Shang, Ling;  Wang, Jian;  Wang, Kai;  Zhou, Jia 收藏  |  浏览/下载：32/0  |  提交时间：2019/12/05 monochorionic diamniotic  placenta  growth discordance  RNA sequencing  leptin  ARMS2   Application of Single-Molecule Amplification and Resequencing Technology for Broad Surveillance of Plasma Mutations in Patients with Advanced Lung Adenocarcinoma 期刊论文 2017, 卷号: 19, 期号: 1, 页码: 169-181 作者:  Wang, Zheng;  Cheng, Gang;  Han, Xiaohong;  Mu, Xinlin;  Zhang, Yuhui 收藏  |  浏览/下载：26/0  |  提交时间：2020/01/03 Molecular analysis of DNA in blastocoele fluid using next-generation sequencing 期刊论文 JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2016, 卷号: 33, 期号: 5 作者:  Zhang, Yixin;  Li, Na;  Wang, Li;  Sun, Huiying;  Ma, Minyue 收藏  |  浏览/下载：32/0  |  提交时间：2019/12/04 Blastocoele fluid  Blastomere  Next-generation sequencing  Preimplantation genetic testing  Bioinformatics   Clinical application of next-generation sequencing in preimplantation genetic diagnosis cycles for Robertsonian and reciprocal translocations 期刊论文 JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2016, 卷号: 33, 期号: 7 作者:  Zhang, Wenke;  Liu, Ying;  Wang, Li;  Wang, Hui;  Ma, Minyue 收藏  |  浏览/下载：32/0  |  提交时间：2019/12/04 Aneuploidy  Copy number variation  Next-generation sequencing  Preimplantation genetic diagnosis  Whole genome amplification   Monochorionic twins with unequal placental sharing: why can the outcome still be favorable? 期刊论文 JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2016, 卷号: 29, 期号: 8 作者:  Sun, Lu-Ming;  Li, Ying;  Zou, Gang;  Zhou, Fenghe;  Lei, Xiaoping 收藏  |  浏览/下载：27/0  |  提交时间：2019/12/05 Monochorionic diamniotic  placental anastomoses  placental injection  uncomplicated   Quantitation of fetal DNA fraction in maternal plasma using circulating single molecule amplification and re-sequencing technology (cSMART) 期刊论文 2016, 卷号: 456, 页码: 151-156 作者:  Song, Yijun;  Zhou, Xiya;  Huang, Saiqiong;  Li, Xiaohong;  Qi, Qingwei 收藏  |  浏览/下载：34/0  |  提交时间：2020/01/04 Circulating single molecule amplification and re-sequencing technology  fetal fraction  Noninvasive prenatal diagnosis  Single nucleotide polymorphism   Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid 期刊论文 2016, 卷号: 36, 期号: 6, 页码: 576-583 作者:  Qi, Qingwei;  Lu, Sijia;  Zhou, Xiya;  Yao, Fengxia;  Hao, Na 收藏  |  浏览/下载：26/0  |  提交时间：2020/01/04