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...
Main Authors: | Roberta Milone, Raffaella Tancredi, Angela Cosenza, Anna Rita Ferrari, Roberta Scalise, Giovanni Cioni, Roberta Battini |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-10-01
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Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/12/11/1660 |
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