Prenatal diagnosis of mosaic trisomy 2 and literature review

BACKGROUND: We presented two cases of mosaic trisomy 2 with high risk of maternal serum screening and non-invasive prenatal testing (NIPT). The invasive amniocentesis was performed and genetic tests including karyotype, single nucleotide polymorphism array(SNP-array), interphase fluorescence in situ...

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Detalles Bibliográficos
Autores principales: Wang, Ting, Lian, Jufei, Ren, Congmian, Huang, Huamei, Huang, Yanlin, Xu, Ling, Zheng, Laiping, Cai, Chanhui, Guo, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445897/
https://www.ncbi.nlm.nih.gov/pubmed/32855656
http://dx.doi.org/10.1186/s13039-020-00504-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445897/
https://www.ncbi.nlm.nih.gov/pubmed/32855656
http://dx.doi.org/10.1186/s13039-020-00504-3

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