Amniocentesis and Next Generation Sequencing (NGS)-Based Noninvasive Prenatal DNA Testing (NIPT) for Prenatal Diagnosis of Fetal Chromosomal Disorders

OBJECTIVE: The present study aimed to evaluate and analyze the results of karyotyping by amniocentesis and next generation sequencing (NGS)-based noninvasive prenatal DNA testing (NIPT) for the prenatal diagnosis of fetal chromosomal disorders. METHODS: A total of 2267 high-risk pregnant females wit...

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Detalles Bibliográficos
Autores principales: Qi, Qi-Ge, Tuo, Ya, Liu, Li-Xue, Yu, Cong-Xiang, Wu, Ai-Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132573/
https://www.ncbi.nlm.nih.gov/pubmed/34025125
http://dx.doi.org/10.2147/IJGM.S297585

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132573/
https://www.ncbi.nlm.nih.gov/pubmed/34025125
http://dx.doi.org/10.2147/IJGM.S297585

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