Incidental Detection of a Chromosomal Aberration by Array-CGH in an Early Prenatal Diagnosis for Monogenic Disease on Coelomic Fluid

Background: Turner syndrome is a rare genetic condition in which a female is partly or completely missing an X chromosome. Signs and symptoms vary among those affected. In fetuses that survive at birth and without congenital malformations, the prognosis is usually positive, but it has high lethality...

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Detalles Bibliográficos
Autores principales: Vinciguerra, Margherita, Leto, Filippo, Cassarà, Filippo, Tartaglia, Viviana, Malacarne, Michela, Coviello, Domenico, Cigna, Valentina, Orlandi, Emanuela, Picciotto, Francesco, Cucinella, Gaspare, Salzano, Emanuela, Piccione, Maria, Maggio, Aurelio, Giambona, Antonino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863495/
https://www.ncbi.nlm.nih.gov/pubmed/36675969
http://dx.doi.org/10.3390/life13010020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863495/
https://www.ncbi.nlm.nih.gov/pubmed/36675969
http://dx.doi.org/10.3390/life13010020

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