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Palabras clave – provistas por la editorial

n/a; screening; single nucleotide polymorphism; predictive and preventive approach; PTEN; cell-free DNAs; fetal fraction; gestational hypertension; RASSF1; CDH1; RT-PCR; cfDNA; statistical models; hematopoietic stem cell transplantation; NanoString; solid organ transplantation; copy number variants; sarcomas; liquid biopsy; obesity; fetal DNA; neutrophil extracellular traps; mammography; non-invasive prenatal testing; ovarian cancer; circulating miRNA; pyrosequencing; growth retardation; preeclampsia; gestational diabetes mellitus; biomarker; inflammatory bowel disease; multi-level diagnostics; PAX1; population study; nuclease activity; NETosis; omics; piRNA; cell-free DNA; prediction; leiomyosarcomas; network analysis; NGS; statistical methods; circulating nucleic acids; deletion/insertion polymorphism; gender differences; leiomyomas; fetal growth restriction; blood plasma; exosomes; miRNA; pregnancy-related complications; NIPT; genetic marker; cell-free nucleic acids; extracellular vesicles; expression; next generation sequencing; breast cancer; individualized patient profile; circulating tumor cells; maternal serum screening; personalized medicine; embryo culture medium; C19MC microRNA; DNA; cell-free RNAs; z-score; fetal cells; microchimerism; aging; plasma