Detection of complex deletions in chromosomes 13 and 21 in a fetus by noninvasive prenatal testing

BACKGROUND: To detect complex fetal subchromosomal abnormalities by noninvasive prenatal testing (NIPT). CASE PRESENTATION: After routine prenatal serum screening, the plasma of high-risk pregnant women were tested via NIPT, and the NIPT results were further validated by fetal karyotype analysis and...

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Detalles Bibliográficos
Autores principales: Wang, Ting, Duan, Chengying, Shen, Cong, Xiang, Jingjing, He, Quanze, Ding, Jie, Wen, Ping, Zhang, Qin, Wang, Wei, Liu, Minjuan, Li, Hong, Li, Haibo, Zhang, Lili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709980/
https://www.ncbi.nlm.nih.gov/pubmed/26759606
http://dx.doi.org/10.1186/s13039-016-0213-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709980/
https://www.ncbi.nlm.nih.gov/pubmed/26759606
http://dx.doi.org/10.1186/s13039-016-0213-4

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