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Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype-Phenotype Correlation.
Genes (Basel). 2022 Nov 10;13(11):2083. doi: 10.3390/genes13112083.
Genes (Basel). 2022.
PMID: 36360320
Free PMC article.
Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review.
Gavril EC, Nucă I, Pânzaru MC, Ivanov AV, Mihai CT, Antoci LM, Ciobanu CG, Rusu C, Popescu R.
Gavril EC, et al. Among authors: nuca i.
Genes (Basel). 2023 Feb 11;14(2):465. doi: 10.3390/genes14020465.
Genes (Basel). 2023.
PMID: 36833393
Free PMC article.
Review.
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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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