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Genetic diagnosis in first or second trimester pregnancy loss using exome sequencing: a systematic review of human essential genes.

Sarah M RobbinsMatthew A ThimmDavid ValleAngie C Jelin
Published in: Journal of assisted reproduction and genetics (2019)
For future studies of RPL, we recommend trio-based ES in cases with normal parental karyotypes. In vitro fertilization with preimplantation genetic diagnosis can be pursued if causative variants are found. Utilization of other sequencing technologies in concert with ES should improve understanding of the causes of early embryonic lethality in humans.
Keyphrases
  • copy number
  • genome wide
  • preterm birth
  • single cell
  • endothelial cells
  • pregnancy outcomes
  • dna methylation
  • induced pluripotent stem cells
  • gene expression
  • pregnant women
  • genome wide identification