Sequential application of copy number variation sequencing and quantitative fluorescence polymerase chain reaction in genetic analysis of miscarriage and stillbirth

BACKGROUND: Copy number variation sequencing (CNV‐seq) could detect most chromosomal abnormalities except polyploidy, and quantitative fluorescence polymerase chain reaction (QF‐PCR) is a supplementary method to CNV‐seq in triploid detection. This study aimed to evaluate the feasibility of sequentia...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Quan, Zhang, Hao, Li, Xue, Li, Junxing, Chen, Huijuan, Liu, Lin, Zhou, Shijie, Xu, Zhihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422063/
https://www.ncbi.nlm.nih.gov/pubmed/37073418
http://dx.doi.org/10.1002/mgg3.2187

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422063/
https://www.ncbi.nlm.nih.gov/pubmed/37073418
http://dx.doi.org/10.1002/mgg3.2187

Ejemplares similares