MLPA as a genetic assay for the prenatal diagnosis of common aneuploidy: the first Egyptian experience

BACKGROUND: The prenatal diagnosis of syndromes caused by chromosomal abnormality is a long-established part of obstetric care. Several DNA-based molecular approaches have provided rapid prenatal diagnosis of of cytogenomic abnormalities. MLPA has become available for rapid aneuploidy detection of t...

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Detalles Bibliográficos
Autores principales: Eid, Ola M., Eid, Maha M., Farid, Marwa, Abdel Kader, Rania M. A., Mahrous, Rana, El-Dessouky, Sara H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334468/
https://www.ncbi.nlm.nih.gov/pubmed/35900681
http://dx.doi.org/10.1186/s43141-022-00402-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334468/
https://www.ncbi.nlm.nih.gov/pubmed/35900681
http://dx.doi.org/10.1186/s43141-022-00402-8

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