Rare genetic variants suggest dysregulation of signaling pathways in low- and high-risk patients developing severe ovarian hyperstimulation syndrome

PURPOSE: To investigate if rare gene variants in women with severe ovarian hyperstimulation syndrome (OHSS) provide clues to the mechanisms involved in the syndrome. METHODS: Among participants in a prospective randomized study (Toftager et al. 2016), six women with predicted low and six women with...

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Bibliografske podrobnosti
izdano v:J Assist Reprod Genet
Main Authors: Borgwardt, L., Olsen, K. W., Rossing, M., Helweg-Larsen, R. Borup, Toftager, M., Pinborg, A., Bogstad, J., Løssl, K., Zedeler, A., Grøndahl, M. L.
Format: Artigo
Jezik:Inglês
Izdano: Springer US 2020
Teme:
Genetics
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7642034/
https://ncbi.nlm.nih.gov/pubmed/32945993
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-020-01941-0
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