Identifying normal embryos from reciprocal translocation carriers by whole chromosome haplotyping

查看全文 作　　者：Zhiqiang [1,2,3,4]Yan;Yuqian [1,2,5]Wang;Yanli [1,2,5]Nie;Xu [1,2,5]Zhi;Xiaohui [1,2,5]Zhu;Meng [1,2,5]Qin;Shuo [1,2,5]Guan;Yixin [1,2,5]Ren;Ying [1,2,5]Kuo;Di [1,2,5]Chang;Wei [1,2,3,4]Chen;Peng [1,2,5]Yuan;Liying [1,2,5]Yan;Jie [1,2,3,5,6]Qiao

机构地区：[1]Center for Reproductive Medicine, Department of Obstetrics andGynecology, Peking University Third Hospital, Beijing 100191, China;[2]Key Laboratory of Assisted Reproduction, Ministry of Education, Beijing 100191, China;[3]Peking-Tsinghua Center for Life Sciences, Peking University, Belting 100871, China;[4]Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China;[5]Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproduction, Beijing 100191, China;[6]Beijing Advanced Innovation Center for Genomics (ICG), Peking University, Beijing 100871, China

出　　处：《Journal of Genetics and Genomics》索引2018年第45卷第9期,共4页

基　　金：supported by the National Natural Science Foundation of China (No. 31522034);Ministry of Science and Technology of China (2016YFC0900103);the National High Technology Research and Development Program Grant (2015AA020407) 摘　　要：Reciprocal translocation is a chromosomal structural abnormality that arises when two non-homologous chromosomes rearrange and attach with each other, an incidence that occurs in about 1/500to 1/625 newborns (Mackie and Scriven, 2002). This event typically does not lead to any significant loss of genetic material, thus reciprocal translocation carriers do not exhibit any severe 关键词：染色体搬运胚胎识别新生儿反常基因

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Identifying normal embryos from reciprocal translocation carriers by whole chromosome haplotyping

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