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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Dades bibliogràfiques
Publicat a:Mol Cytogenet
Autors principals: Wang, Ting, Lian, Jufei, Ren, Congmian, Huang, Huamei, Huang, Yanlin, Xu, Ling, Zheng, Laiping, Cai, Chanhui, Guo, Li
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2020
Matèries:
Research
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7445897/
https://ncbi.nlm.nih.gov/pubmed/32855656
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-020-00504-3
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