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Page 1
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.
Genes (Basel). 2022 Nov 10;13(11):2083. doi: 10.3390/genes13112083.
Genes (Basel). 2022.
PMID: 36360320
Free PMC article.
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Genetics of Hearing Impairment in North-Eastern Romania-A Cost-Effective Improved Diagnosis and Literature Review.
Resmerita I, Cozma RS, Popescu R, Radulescu LM, Panzaru MC, Butnariu LI, Caba L, Ilie OD, Gavril EC, Gorduza EV, Rusu C.
Resmerita I, et al. Among authors: gavril ec.
Genes (Basel). 2020 Dec 15;11(12):1506. doi: 10.3390/genes11121506.
Genes (Basel). 2020.
PMID: 33333757
Free PMC article.
Review.
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Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review.
Gavril EC, Luca AC, Curpan AS, Popescu R, Resmerita I, Panzaru MC, Butnariu LI, Gorduza EV, Gramescu M, Rusu C.
Gavril EC, et al.
Children (Basel). 2021 Aug 30;8(9):751. doi: 10.3390/children8090751.
Children (Basel). 2021.
PMID: 34572183
Free PMC article.
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