New Insights in 9q21.13 Microdeletion Syndrome: Genotype–Phenotype Correlation of 28 Patients

The implementation of array comparative genomic hybridisation (array-CGH) allows us to describe new microdeletion/microduplication syndromes which were previously not identified. 9q21.13 microdeletion syndrome is a genetic condition due to the loss of a critical genomic region of approximately 750kb...

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Detalles Bibliográficos
Autores principales: De Falco, Alessandro, Iolascon, Achille, Ascione, Flora, Piscopo, Carmelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218196/
https://www.ncbi.nlm.nih.gov/pubmed/37239476
http://dx.doi.org/10.3390/genes14051116

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218196/
https://www.ncbi.nlm.nih.gov/pubmed/37239476
http://dx.doi.org/10.3390/genes14051116

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