Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review

Chromosome 9p deletion syndrome is a rare autosomal dominant disorder presenting with a broad spectrum of clinical features, including congenital heart defects (CHDs). To date, studies focused on a deep characterization of cardiac phenotype and function associated with this condition are lacking. We...

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Detalles Bibliográficos
Autores principales: Pugnaloni, Flaminia, Onesimo, Roberta, Blandino, Rita, Putotto, Carolina, Versacci, Paolo, Delogu, Angelica Bibiana, Leoni, Chiara, Trevisan, Valentina, Croci, Ileana, Calì, Federica, Digilio, Maria Cristina, Zampino, Giuseppe, Marino, Bruno, Calcagni, Giulio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859094/
https://www.ncbi.nlm.nih.gov/pubmed/36672887
http://dx.doi.org/10.3390/genes14010146

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859094/
https://www.ncbi.nlm.nih.gov/pubmed/36672887
http://dx.doi.org/10.3390/genes14010146

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