Maternal Malignancy After Atypical Findings on Single-Nucleotide Polymorphism–Based Prenatal Cell-Free DNA Screening

To evaluate the incidence and clinical outcomes of cell-free DNA results suspicious for maternal malignancy on prenatal cell-free DNA screening with single-nucleotide polymorphism (SNP)–based technology. METHODS: This retrospective cohort study included data from SNP-based, noninvasive prenatal scre...

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Detalles Bibliográficos
Autores principales: Goldring, Georgina, Trotter, Cindy, Meltzer, Jeffrey T., Souter, Vivienne, Pais, Lynn, DiNonno, Wendy, Xu, Wenbo, Weitzel, Jeffrey N., Vora, Neeta L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Obstetrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026947/
https://www.ncbi.nlm.nih.gov/pubmed/36897127
http://dx.doi.org/10.1097/AOG.0000000000005107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026947/
https://www.ncbi.nlm.nih.gov/pubmed/36897127
http://dx.doi.org/10.1097/AOG.0000000000005107

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