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Copy number variations in patients with idiopathic recurrent pregnancy loss: an array-CGH approach

BACKGROUND/AIM: It is not always possible to determine the causative basis of pregnancy losses and even today it has been reported that 50% of cases with recurrent pregnancy loss (RPL) have no reason to be detected. In our study, it is aimed to reveal the copy number variations (CNVs) of the genes w...

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Detalles Bibliográficos
Autores principales: YILDIZ, Onur, SILAN, Fatma, KARAKAYA, Taner, ÖZDEMİR, Öztürk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific and Technological Research Council of Turkey (TUBITAK) 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395738/
https://www.ncbi.nlm.nih.gov/pubmed/36422498
http://dx.doi.org/10.55730/1300-0144.5511

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