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Year | Number of Results |
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2010 | 2 |
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Page 1
Developments in Genetics: Better Management of Ovarian Cancer Patients.
Int J Mol Sci. 2023 Nov 5;24(21):15987. doi: 10.3390/ijms242115987.
Int J Mol Sci. 2023.
PMID: 37958970
Free PMC article.
Review.
Homologous Recombination Deficiency Score Determined by Genomic Instability in a Romanian Cohort.
Rădoi VE, Țurcan M, Maioru OV, Dan A, Bohîlțea LC, Dumitrescu EA, Gheorghe AS, Stănculeanu DL, Thodi G, Loukas YL, Săbău ID.
Rădoi VE, et al. Among authors: bohiltea lc.
Diagnostics (Basel). 2023 May 29;13(11):1896. doi: 10.3390/diagnostics13111896.
Diagnostics (Basel). 2023.
PMID: 37296748
Free PMC article.
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Risk of Death in Comorbidity Subgroups of Hospitalized COVID-19 Patients Inferred by Routine Laboratory Markers of Systemic Inflammation on Admission: A Retrospective Study.
Cocoş R, Mahler B, Turcu-Stiolica A, Stoichiță A, Ghinet A, Shelby ES, Bohîlțea LC.
Cocoş R, et al. Among authors: bohiltea lc.
Viruses. 2022 May 31;14(6):1201. doi: 10.3390/v14061201.
Viruses. 2022.
PMID: 35746672
Free PMC article.
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The importance of screening and prenatal diagnosis in the identification of the numerical chromosomal abnormalities.
Neagos D, Cretu R, Sfetea RC, Bohiltea LC.
Neagos D, et al. Among authors: bohiltea lc.
Maedica (Bucur). 2011 Jul;6(3):179-84.
Maedica (Bucur). 2011.
PMID: 22368694
Free PMC article.
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RFC - 1 Gene Polymorphism and the Risk of Down Syndrome in Romanian Population.
Neagos D, Cretu R, Tutulan-Cunita A, Stoian V, Bohiltea LC.
Neagos D, et al. Among authors: bohiltea lc.
Maedica (Bucur). 2010 Dec;5(4):280-5.
Maedica (Bucur). 2010.
PMID: 21977171
Free PMC article.
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Genotype-phenotype correlations in a mountain population community with high prevalence of Wilson's disease: genetic and clinical homogeneity.
Cocoş R, Şendroiu A, Schipor S, Bohîlţea LC, Şendroiu I, Raicu F.
Cocoş R, et al. Among authors: bohiltea lc.
PLoS One. 2014 Jun 4;9(6):e98520. doi: 10.1371/journal.pone.0098520. eCollection 2014.
PLoS One. 2014.
PMID: 24897373
Free PMC article.
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Methylenetetrahydrofolate dehydrogenase (MTHFD) enzyme polymorphism as a maternal risk factor for trisomy 21: a clinical study.
Neagos D, Cretu R, Tutulan-Cunita A, Stoian V, Bohiltea LC.
Neagos D, et al. Among authors: bohiltea lc.
J Med Life. 2010 Oct-Dec;3(4):454-7.
J Med Life. 2010.
PMID: 21254748
Free PMC article.
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