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Identifying normal embryos from reciprocal translocation carriers by whole chromosome haplotyping

Zhiqiang Yan Yuqian Wang Yanli Nie Xu Zhi Xiaohui Zhu Meng Qin Shuo Guan Yixin Ren Ying Kuo Di Chang Wei Chen Peng Yuan Liying Yan Jie Qiao

Zhiqiang Yan, Yuqian Wang, Yanli Nie, Xu Zhi, Xiaohui Zhu, Meng Qin, Shuo Guan, Yixin Ren, Ying Kuo, Di Chang, Wei Chen, Peng Yuan, Liying Yan, Jie Qiao. Identifying normal embryos from reciprocal translocation carriers by whole chromosome haplotyping[J]. Journal of Genetics and Genomics, 2018, 45(9): 505-508. doi: 10.1016/j.jgg.2018.05.006
Citation: Zhiqiang Yan, Yuqian Wang, Yanli Nie, Xu Zhi, Xiaohui Zhu, Meng Qin, Shuo Guan, Yixin Ren, Ying Kuo, Di Chang, Wei Chen, Peng Yuan, Liying Yan, Jie Qiao. Identifying normal embryos from reciprocal translocation carriers by whole chromosome haplotyping[J]. Journal of Genetics and Genomics, 2018, 45(9): 505-508. doi: 10.1016/j.jgg.2018.05.006

doi: 10.1016/j.jgg.2018.05.006

Identifying normal embryos from reciprocal translocation carriers by whole chromosome haplotyping

More Information
  • [1] Fiorentino, F., Spizzichino, L., Bono, S. et al. PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization Hum. Reprod., 26 (2011),pp. 1925-1935
    [2] Fischer, J., Colls, P., Escudero, T. et al. Preimplantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses Fertil. Steril., 94 (2010),pp. 283-289
    [3] Hu, L., Cheng, D., Gong, F. et al. Reciprocal translocation carrier diagnosis in preimplantation human embryos EBioMedicine, 14 (2016),pp. 139-147
    [4] Li, G., Jin, H., Xin, Z. et al. Increased IVF pregnancy rates after microarray preimplantation genetic diagnosis due to parental translocations Syst. Biol. Reprod. Med., 60 (2014),pp. 119-124
    [5] Mackie, O.C., Scriven, P.N. Meiotic outcomes in reciprocal translocation carriers ascertained in 3-day human embryos Eur. J. Hum. Genet., 10 (2002),pp. 801-806
    [6] Scriven, P.N., Handyside, A.H., Ogilvie, C.M. Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis Prenat. Diagn., 18 (1998),pp. 1437-1449
    [7] Treff, N.R., Thompson, K., Rafizadeh, M. et al. SNP array-based analyses of unbalanced embryos as a reference to distinguish between balanced translocation carrier and normal blastocysts J. Assist. Reprod. Genet., 33 (2016),pp. 1115-1119
    [8] van Uum, C.M., Stevens, S.J., Dreesen, J.C. et al. SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations Eur. J. Hum. Genet., 20 (2012),pp. 938-944
    [9] Xu, J., Fang, R., Chen, L. et al. Proc. Natl. Acad. Sci. U. S. A., 113 (2016),pp. 11907-11912
    [10] Xu, J., Zhang, Z., Niu, W. et al. Mapping allele with resolved carrier status of Robertsonian and reciprocal translocation in human preimplantation embryos Proc. Natl. Acad. Sci. U. S. A., 114 (2017),pp. E8695-E8702
    [11] Yan, L., Huang, L., Xu, L. et al. Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses Proc. Natl. Acad. Sci. U. S. A., 112 (2015),pp. 15964-15969
    [12] Zhang, W., Liu, Y., Wang, L. et al. Clinical application of next-generation sequencing in preimplantation genetic diagnosis cycles for Robertsonian and reciprocal translocations J. Assist. Reprod. Genet., 33 (2016),pp. 899-906
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出版历程
  • 收稿日期:  2018-01-25
  • 录用日期:  2018-05-13
  • 修回日期:  2018-03-28
  • 网络出版日期:  2018-07-11
  • 刊出日期:  2018-09-20

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