Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders

BACKGROUND: High-cost, time-consuming and complex processes of several current approaches limit the use of noninvasive prenatal diagnosis (NIPD) for monogenic disorders in clinical application. Thus, a more cost-effective and easily implementable approach is required. METHODS: We established a low-c...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Wenman, Zhou, Xuanyou, Jiang, Zhengwen, Zhang, Dazhi, Yu, Feng, Zhang, Lanlan, Wang, Xuefeng, Chen, Songchang, Xu, Chenming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327225/
https://www.ncbi.nlm.nih.gov/pubmed/35897115
http://dx.doi.org/10.1186/s40246-022-00400-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327225/
https://www.ncbi.nlm.nih.gov/pubmed/35897115
http://dx.doi.org/10.1186/s40246-022-00400-4

Ejemplares similares