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Volume 45 Issue 9
Sep.  2018
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Article Contents

Identifying normal embryos from reciprocal translocation carriers by whole chromosome haplotyping

doi: 10.1016/j.jgg.2018.05.006
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  • Corresponding author: E-mail address: yanliyingkind@aliyun.com (Liying Yan); E-mail address: jie.qiao@263.net (Jie Qiao)
  • Received Date: 2018-01-25
  • Accepted Date: 2018-05-13
  • Rev Recd Date: 2018-03-28
  • Available Online: 2018-07-11
  • Publish Date: 2018-09-20
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    [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
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    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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