17q12 Recurrent Deletions and Duplications: Description of a Case Series with Neuropsychiatric Phenotype

Syndromic neurodevelopmental disorders are usually investigated through genetics technologies, within which array comparative genomic hybridization (Array-CGH) is still considered the first-tier clinical diagnostic test. Among recurrent syndromic imbalances, 17q12 deletions and duplications are char...

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Detalles Bibliográficos
Autores principales: Milone, Roberta, Tancredi, Raffaella, Cosenza, Angela, Ferrari, Anna Rita, Scalise, Roberta, Cioni, Giovanni, Battini, Roberta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620923/
https://www.ncbi.nlm.nih.gov/pubmed/34828266
http://dx.doi.org/10.3390/genes12111660

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620923/
https://www.ncbi.nlm.nih.gov/pubmed/34828266
http://dx.doi.org/10.3390/genes12111660

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