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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.
The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients.
Budisteanu M, Papuc SM, Streata I, Cucu M, Pirvu A, Serban-Sosoi S, Erbescu A, Andrei E, Iliescu C, Ioana D, Severin E, Ioana M, Arghir A.
Budisteanu M, et al. Among authors: serban sosoi s.
Genes (Basel). 2021 Jul 1;12(7):1025. doi: 10.3390/genes12071025.
Genes (Basel). 2021.
PMID: 34356041
Free PMC article.
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Array CGH - A Powerful Tool in Molecular Diagnostic of Pathogenic Microdeletions - Williams-Beuren Syndrome - A Case Report.
Streață I, Șerban-Șoșoi S, Budișteanu M, Pîrvu A, Burada F, Mixich F, Ioana M.
Streață I, et al. Among authors: serban sosoi s.
Curr Health Sci J. 2016 Apr-Jun;42(2):207-212. doi: 10.12865/CHSJ.42.02.14. Epub 2016 Jun 28.
Curr Health Sci J. 2016.
PMID: 30568834
Free PMC article.
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Prenatal diagnosis of a pure 15q distal trisomy derived from a maternal pericentric inversion: A case report.
Burada F, Streata I, Ungureanu A, Ruican D, Nagy R, Serban-Sosoi S, Stambouli D, Dimos L, Popescu-Hobeanu G, Mihai I, Iliescu D.
Burada F, et al. Among authors: serban sosoi s.
Exp Ther Med. 2021 Apr;21(4):304. doi: 10.3892/etm.2021.9735. Epub 2021 Jan 29.
Exp Ther Med. 2021.
PMID: 33717247
Free PMC article.
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Determination of autophagy gene ATG16L1 polymorphism in human colorectal cancer.
Nicoli ER, Dumitrescu T, Uscatu CD, Popescu FD, Streaţă I, Serban Şoşoi S, Ivanov P, Dumitrescu A, Bărbălan A, Lungulescu D, Petrescu F, Schenker M, Verdeş D, Săftoiu A.
Nicoli ER, et al. Among authors: serban sosoi s.
Rom J Morphol Embryol. 2014;55(1):57-62.
Rom J Morphol Embryol. 2014.
PMID: 24715166
Free article.
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Impact of Intermediate Hyperglycemia and Diabetes on Immune Dysfunction in Tuberculosis.
Eckold C, Kumar V, Weiner J, Alisjahbana B, Riza AL, Ronacher K, Coronel J, Kerry-Barnard S, Malherbe ST, Kleynhans L, Stanley K, Ruslami R, Ioana M, Ugarte-Gil C, Walzl G, van Crevel R, Wijmenga C, Critchley JA, Dockrell HM, Cliff JM; TANDEM consortium.
Eckold C, et al.
Clin Infect Dis. 2021 Jan 23;72(1):69-78. doi: 10.1093/cid/ciaa751.
Clin Infect Dis. 2021.
PMID: 32533832
Free PMC article.
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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: serban sosoi s.
Diagnostics (Basel). 2022 Dec 12;12(12):3137. doi: 10.3390/diagnostics12123137.
Diagnostics (Basel). 2022.
PMID: 36553144
Free PMC article.
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