Detection of cytogenomic abnormalities by OncoScan microarray assay for products of conception from formalin-fixed paraffin-embedded and fresh fetal tissues

BACKGROUND: The OncoScan microarray assay (OMA) using highly multiplexed molecular inversion probes for single nucleotide polymorphism (SNP) loci enabled the detection of cytogenomic abnormalities of chromosomal imbalances and pathogenic copy number variants (pCNV). The small size of molecular inver...

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Detalles Bibliográficos
Autores principales: Wen, Jiadi, Grommisch, Brittany, DiAdamo, Autumn, Chai, Hongyan, Ng, Sok Meng Evelyn, Hui, Pei, Bale, Allen, Mak, Winifred, Wang, Guilin, Li, Peining
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019165/
https://www.ncbi.nlm.nih.gov/pubmed/33810806
http://dx.doi.org/10.1186/s13039-021-00542-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019165/
https://www.ncbi.nlm.nih.gov/pubmed/33810806
http://dx.doi.org/10.1186/s13039-021-00542-5

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