Single-cell whole-genome sequencing, haplotype analysis in prenatal diagnosis of monogenic diseases

Monogenic inherited diseases are common causes of congenital disabilities, leading to severe economic and mental burdens on affected families. In our previous study, we demonstrated the validity of cell-based noninvasive prenatal testing (cbNIPT) in prenatal diagnosis by single-cell targeted sequenc...

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Detalles Bibliográficos
Autores principales: Chang, Liang, Jiao, Haining, Chen, Jiucheng, Wu, Guanlin, Liu, Ping, Li, Rong, Guo, Jianying, Long, Wenqing, Tang, Xiaojian, Lu, Bingjie, Xu, Haibin, Wu, Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2023
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947115/
https://www.ncbi.nlm.nih.gov/pubmed/36810160
http://dx.doi.org/10.26508/lsa.202201761

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947115/
https://www.ncbi.nlm.nih.gov/pubmed/36810160
http://dx.doi.org/10.26508/lsa.202201761

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