Prenatal genetic diagnosis of monogenic diseases

Prenatal genetic diagnosis of monogenic diseases is a process involving the use of a variety of molecular techniques for the molecular characterization of a potential monogenic disease in the fetus during pregnancy. Prenatal genetic diagnosis can be performed through invasive and non-invasive method...

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Detalles Bibliográficos
Autores principales: Prior-de Castro, Carmen, Gómez-González, Clara, Rodríguez-López, Raquel, Macher, Hada C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197187/
https://www.ncbi.nlm.nih.gov/pubmed/37359899
http://dx.doi.org/10.1515/almed-2023-0024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197187/
https://www.ncbi.nlm.nih.gov/pubmed/37359899
http://dx.doi.org/10.1515/almed-2023-0024

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