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Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review.
Genes (Basel). 2023 Feb 11;14(2):465. doi: 10.3390/genes14020465.
Genes (Basel). 2023.
PMID: 36833393
Free PMC article.
Review.
Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype-Phenotype Correlation.
Gavril EC, Popescu R, Nucă I, Ciobanu CG, Butnariu LI, Rusu C, Pânzaru MC.
Gavril EC, et al. Among authors: nuca i.
Genes (Basel). 2022 Nov 10;13(11):2083. doi: 10.3390/genes13112083.
Genes (Basel). 2022.
PMID: 36360320
Free PMC article.
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BRAF V600E Mutation in Malignant Melanoma-A Romanian Research Experience.
Avădănei ER, Căruntu ID, Nucă I, Balan R, Lozneanu L, Giusca SE, Amalinei C.
Avădănei ER, et al. Among authors: nuca i.
Medicina (Kaunas). 2024 Feb 20;60(3):351. doi: 10.3390/medicina60030351.
Medicina (Kaunas). 2024.
PMID: 38541077
Free PMC article.
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Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome.
Ciobanu CG, Nucă I, Popescu R, Antoci LM, Caba L, Ivanov AV, Cojocaru KA, Rusu C, Mihai CT, Pânzaru MC.
Ciobanu CG, et al. Among authors: nuca i.
Int J Mol Sci. 2023 May 24;24(11):9206. doi: 10.3390/ijms24119206.
Int J Mol Sci. 2023.
PMID: 37298158
Free PMC article.
Review.
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