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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific and Technological Research Council of Turkey (TUBITAK)
2022
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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 |