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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2021
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| Materias: | |
| 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 |