Clinical re-biopsy of segmental gains—the primary source of preimplantation genetic testing false positives

被引:0
作者
Steve Grkovic
Maria V. Traversa
Mark Livingstone
Steven J. McArthur
机构
[1] Genea,
来源
Journal of Assisted Reproduction and Genetics | 2022年 / 39卷
关键词
Mosaicism; Preimplantation genetic testing; Segmental aneuploidy; False positives; Clinical re-biopsy;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:1313 / 1322
页数:9
相关论文
共 150 条
  • [1] Girardi L(2020)Incidence, origin, and predictive model for the detection and clinical management of segmental aneuploidies in human embryos Am J Hum Genet 106 525-534
  • [2] Serdarogullari M(2009)De novo balanced chromosome rearrangements in prenatal diagnosis Prenat Diagn 29 257-265
  • [3] Patassini C(2018)Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta-analysis Ultrasound Obstet Gynecol 51 445-452
  • [4] Poli M(2012)Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe Eur J Hum Genet 20 521-526
  • [5] Fabiani M(2019)One hundred mosaic embryos transferred prospectively in a single clinic: exploring when and why they result in healthy pregnancies Fertil Steril 111 280-293
  • [6] Caroselli S(2020)Concordance of various chromosomal errors among different parts of the embryo and the value of re-biopsy in embryos with segmental aneuploidies Mol Hum Reprod 26 269-276
  • [7] Giardino D(2019)The clinicianś dilemma with mosaicism - an insight from inner cell mass biopsies Hum Reprod 34 998-1010
  • [8] Corti C(2018)Prevalence and authenticity of de-novo segmental aneuploidy (>16 Mb) in human blastocysts as detected by next-generation sequencing Reprod Biomed Online 37 511-520
  • [9] Ballarati L(2019)Transfer of embryos with segmental mosaicism is associated with a significant reduction in live-birth rate Fertil Steril 111 69-76
  • [10] Colombo D(2020)The pregnancy outcome of mosaic embryo transfer: A prospective multicenter study and meta-analysis Genes 11 973-4