未登录The uncertainty of copy number variants: pregnancy decisions and clinical follow-up
Shi, Panlai; Liang, Hongbin; Hou, Yaqin; Chen, Duo; Ren, Huanan; Wang, Conghui; Xia, Yanjie; Zhang, Da; Leigh, Don; Cram, David S.; Kong, Xiangdong .png)
分享.png)
收藏PGDIS position statement on the transfer of mosaic embryos 2021PGDIS关于花叶胚胎2021转移的立场声明Leigh, D.; Cram, D. S.; Rechitsky, S.; Handyside, A.; Wells, D.; Munne, S.; Kahraman, S.; Grifo, J.; Katz-Jaffe, M.; Rubio, C.; Viotti, M.; Forman, E.; Xu, K.; Gordon, T.; Madjunkova, S.; Qiao, J.; Chen, Z-J; Harton, G.; Gianaroli, L.; Simon, C.; Scott, R.; Simpson, J. L.; Kuliev, A. 分享 收藏 A More Universal Approach to Comprehensive Analysis of Thalassemia Alleles (CATSA)Liang, Qiaowei; Gu, Wanqian; Chen, Ping; Li, Yuezhen; Liu, Yanqiu; Tian, Mao; Zhou, Qiaomiao; Qi, Hongbo; Zhang, Yuhong; He, Jun; Li, Qing; Tang, Lingfang; Tang, Juan; Teng, Yanling; Zhou, Yulin; Huang, Shengwen; Lu, Zongjie; Xu, Mengnan; Hou, Wei; Huang, Ting; Li, Youqiong; Li, Rong; Hu, Lanping; Li, Shaoying; Guo, Qiwei; Zhuo, Zhaozhen; Mou, Yan; Cram, David S.; Wu, Lingqian 分享 收藏 分享 收藏 Molecular testing for H. pylori clarithromycin and quinolone resistance: a prospective Chinese studyZhang, Chuanfeng; Cao, Mengjiao; Lv, Tangshan; Wang, Hongyan; Liu, Xiaoxiao; Xie, Yong; Lv, Nonghua; Chen, Hongtan; Cram, David S.; Zhong, Jing; Zhou, Linfu 分享 收藏 分享 收藏 分享 收藏 Genetic profiling of primary and secondary tumors from patients with lung adenocarcinoma and bone metastases reveals targeted therapy optionsHuang, Long; Jiang, Xiao-Liu; Liang, Hong-Bin; Li, Jian-Cheng; Chin, Li-Han; Wei, Jian-Ping; Wang, Rui-Ru; Cai, Jing; Xiong, Qiang; Wang, Lien-Tu; Cram, David S.; Liu, An-Wen 分享 收藏 A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and β-Thalassemia CarriersXu, Liangpu; Mao, Aiping; Liu, Hui; Gui, Baoheng; Choy, Kwong W.; Huang, Hailong; Yu, Qian; Zhang, Xiaojie; Chen, Meihuan; Lin, Na; Chen, Lingji; Han, Jin; Wang, Yan; Zhang, Min; Li, Xiaoyu; He, Deqin; Lin, Yuan; Zhang, Jianguang; Cram, David S.; Cao, Hua 分享 收藏 分享 收藏 Analysis of balanced reciprocal translocations in patients with subfertility using single-molecule optical mappingWang, Hui; Jia, Zhengjun; Mao, Aiping; Xu, Bing; Wang, Shuling; Wang, Li; Liu, Sai; Zhang, Haiman; Zhang, Xiaojie; Yu, Tao; Mu, Ting; Xu, Mengnan; Cram, David S.; Yao, Yuanqing 分享 收藏 A New Approach for Preimplantation Testing and Noninvasive Prenatal Diagnosis Confirmation of Fetal GenotypeRechitsky, Svetlana; Kuliev, Anver; San Ramon, Geraldine; Tur-Kaspa, Ilan; Wang, Yin; Wang, Wenjie; Wu, Xueqing; Wang, Li; Leigh, Don; Cram, David S. 分享 收藏 Low-depth whole genome sequencing reveals copy number variations associated with higher pathologic grading and more aggressive subtypes of lung non-mucinous adenocarcinoma低深度全基因组测序揭示拷贝数变异与肺非黏液腺癌更高病理分级和更具侵袭性亚型相关Wang, Zheng; Zhang, Lin; He, Lei; Cui, Di; Liu, Chenglong; Yin, Liangyu; Zhang, Min; Jiang, Lei; Gong, Yuyan; Wu, Wang; Liu, Bi; Li, Xiaoyu; Cram, David S.; Liu, Dongge 分享 收藏 Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromesLiang, Desheng; Cram, David S.; Tan, Hu; Linpeng, Siyuan; Liu, Yingdi; Sun, Huaiyu; Zhang, Yu; Tian, Feng; Zhu, Hongmin; Xu, Mengnan; Wang, Hua; Yu, Fuli; Wu, Lingqian 分享 收藏 PGDIS Position Statement on the Transfer of Mosaic Embryos 2019Cram, D. S.; Leigh, D.; Handyside, A.; Rechitsky, L.; Xu, K.; Harton, G.; Grifo, J.; Rubio, C.; Fragouli, E.; Kahraman, S.; Forman, E.; Katz-Jaffe, M.; Tempest, H.; Thornhill, A.; Strom, C.; Escudero, T.; Qiao, J.; Munne, S.; Simpson, J. L.; Kuliev, A. 分享 收藏 Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing使用拷贝数变异测序对中国3429例羊膜穿刺术样本进行前瞻性染色体分析Wang, Jing; Chen, Lin; Zhou, Cong; Wang, Li; Xie, Hanbing; Xiao, Yuanyuan; Zhu, Hongmei; Hu, Ting; Zhang, Zhu; Zhu, Qian; Liu, Zhiying; Liu, Shanlin; Wang, He; Xu, Mengnan; Ren, Zhilin; Yu, Fuli; Cram, David S.; Liu, Hongqian 分享 收藏 High levels of circulating cell-free DNA are a biomarker of active SLEXu, Yalan; Song, Yijun; Chang, Jiazhen; Zhou, Xiya; Qi, Qingwei; Tian, Xinping; Li, Mengtao; Zeng, Xiaofeng; Xu, Mengnan; Zhang, Wenjuan; Cram, David S.; Liu, Juntao 分享 收藏 分享 收藏 A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutationsHan, Mingyu; Li, Zhifeng; Wang, Wenlu; Huang, Shasha; Lu, Yanping; Gao, Zhiying; Wang, Longxia; Kang, Dongyang; Li, Linwei; Liu, Yiqian; Xu, Mengnan; Cram, David S.; Dai, Pu 分享 收藏 Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early developmentChen, Yiyun; Bartanus, Justin; Liang, Desheng; Zhu, Hongmin; Breman, Amy M.; Smith, Janice L.; Wang, Hua; Ren, Zhilin; Patel, Ankita; Stankiewicz, Pawel; Cram, David S.; Cheung, Sau Wai; Wu, Lingqian; Yu, Fuli 分享 收藏 
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
