Prenatal diagnosis of 7 cases with uniparental disomy by utilization of single nucleotide polymorphism array

BACKGROUND: The phenotypes of uniparental disomy (UPD) are variable, which may either have no clinical impact, lead to clinical signs and symptoms. Molecular analysis is essential for making a correct diagnosis. This study involved a retrospective analysis of 4512 prenatal diagnosis samples and expl...

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Detalles Bibliográficos
Autores principales: Zhou, Lili, Zheng, Zhaoke, Xu, Yunzhi, Lv, Xiaoxiao, Xu, Chenyang, Xu, Xueqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980353/
https://www.ncbi.nlm.nih.gov/pubmed/33741026
http://dx.doi.org/10.1186/s13039-021-00537-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980353/
https://www.ncbi.nlm.nih.gov/pubmed/33741026
http://dx.doi.org/10.1186/s13039-021-00537-2

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