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Expanding the Clinical Phenotype of 19q Interstitial Deletions: A New Case with 19q13.32-q13.33 Deletion and Short Review of the Literature.
Genes (Basel). 2022 Jan 24;13(2):212. doi: 10.3390/genes13020212.
Genes (Basel). 2022.
PMID: 35205257
Free PMC article.
Review.
Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability-Data from a Romanian Cohort.
Streață I, Caramizaru A, Riza AL, Șerban-Sosoi S, Pîrvu A, Cara ML, Cucu MG, Dobrescu AM, Ro-Nmca-Id Group, CExBR Pediatric Neurology Obregia Group, CExBR Pediatric Neurology V Gomoiu Hospital Group, Shelby ES, Albeanu A, Burada F, Ioana M.
Streață I, et al. Among authors: caramizaru a.
Diagnostics (Basel). 2022 Dec 12;12(12):3137. doi: 10.3390/diagnostics12123137.
Diagnostics (Basel). 2022.
PMID: 36553144
Free PMC article.
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