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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...

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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

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