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浏览/检索结果: 共4条，第1-4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 Outcomes of Preimplantation Genetic Diagnosis Cycles by Fluorescent In situ Hybridization of Infertile Males with Nonmosaic 47,XYY Syndrome 期刊论文 CHINESE MEDICAL JOURNAL, 2018, 卷号: 131, 期号: 15, 页码: 1808-1812 作者:  Xu, Chao;  Zhang, Fang-Fang;  Li, Hong-Chang;  Wang, Miao-Miao;  Zhu, Yue-Ting 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/11 47,XYY Syndrome  Fluorescent In situ Hybridization  Infertility  Pregnancy Outcome  Preimplantation Genetic Diagnosis   Outcomes of Preimplantation Genetic Diagnosis Cycles by Fluorescent In situ Hybridization of Infertile Males with Nonmosaic 47,XYY Syndrome 期刊论文 中华医学杂志：英文版, 2018, 期号: 15 作者:  Chao Xu;  Fang-Fang Zhang;  Hong-Chang Li;  Miao-Miao Wang;  Yue-Ting Zhu 收藏  |  浏览/下载：8/0  |  提交时间：2019/12/11 基因诊断  杂交率  症候群  荧光灯  周期  男性  原子核  怀孕率   Preferential Y-Y pairing and synapsis and abnormal meiotic recombination in a 47, XYY man with non obstructive azoospermia 期刊论文 MOLECULAR CYTOGENETICS, 2016, 卷号: 9 作者:  Wu, Caiyun;  Wang, Liu;  Iqbal, Furhan;  Jiang, Xiaohua;  Bukhari, Ihtisham 收藏  |  浏览/下载：16/0  |  提交时间：2019/12/05 Sex chromosomes  Meiosis  Meiotic sex chromosome inactivation (MSCI)  XYY syndrome   A de novo 2q35-q36.1 deletion incorporating IHH in a Chinese boy (47, XYY) with syndactyly, type III waardenburg syndrome, and congenital heart disease 期刊论文 Genetics and Molecular Research, 2016, 卷号: 15, 期号: 4 作者:  Wang, D;  Ren, G F;  Zhang, H Z;  Yi, C Y;  Peng, Z J 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/16 Congenital heart disease  Deletion 2q35-q36.1  IHH  Syndactyly  Type III Waardenburg syndrome