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Explorer les aberrations chromosomiques X dans les cellules ovariennes en utilisant l’hybridation in situ par fluorescence
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Exploring X Chromosomal Aberrations in Ovarian Cells by Using Fluorescence In Situ Hybridization
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Explorer les aberrations chromosomiques X dans les cellules ovariennes en utilisant l’hybridation in situ par fluorescence

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11:08 min

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April 07, 2023

DOI:

10.3791/64734-v

DOI:
10.3791/64734-v

•

11:08 min
April 07, 2023

•

10 Views
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1Department of Obstetrics and Gynecology,Radboudumc, 2Department of Pediatrics,Radboudumc, Amalia Children’s Hospital, 3Department of Reproductive Medicine,Nij Geertgen Center for Fertility

Summary

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Cet article présente deux méthodes basées sur l’hybridation in situ par fluorescence pour déterminer le contenu chromosomique X des cellules ovariennes dans le tissu du cortex ovarien non greffé et greffé de femelles présentant des aberrations chromosomiques X.

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Cite this Article

Nadesapillai, S., van der Velden, J., Braat, D., Fleischer, K., Peek, R. Exploring X Chromosomal Aberrations in Ovarian Cells by Using Fluorescence In Situ Hybridization. J. Vis. Exp. (194), e64734, doi:10.3791/64734 (2023).

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