[1. Jinca C, Petrescu CAM, Boeriu E, Oprisoni A, Balint-Gib L, Baica M, et al. The impact of immunological and biomolecular investigations on the outcome of children with acute lymphoblastic leukemia - experience of IIIrd Paediatric Clinic Timisoara. Rev Romana Med Lab. 2018;26(1):77-85. DOI: 10.1515/rrlm-2017-002910.1515/rrlm-2017-0029]Open DOISearch in Google Scholar
[2. Arber DA, Orazi A, Hasserjian R, Thiele J, Borowitz MJ, Le Beau MM, et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood. 2016 May 19;127(20):2391–405. DOI: 10.1182/blood-2016-03-64354410.1182/blood-2016-03-643544]Open DOISearch in Google Scholar
[3. Döhner H, Estey E, Grimwade D, Amadori S, Appelbaum FR, Büchner T, et al. Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel. Blood. 2017 Jan 26;129(4):424–47 DOI: 10.1182/blood-2016-08-73319610.1182/blood-2016-08-733196]Open DOISearch in Google Scholar
[4. Berbec NP, Papuc SM, Tutulan-Cunita AC, Angelescu SM, Lupu AI, Arghir AA. Molecular characterization of complex chromosomal changes in de novo acute myeloid leukemia: a case report. Rev Romana Med Lab. 2013;21(1):59-65. DOI: 10.2478/rrlm-2013-001810.2478/rrlm-2013-0018]Open DOISearch in Google Scholar
[5. Crauciuc GA, Tripon F, Bogliş A, Făgărăşan A, Bănescu C. Multiplex ligation dependent probe amplification-A useful, fast and cost-effective method for identification of small supernumerary marker chromosome in children with developmental delay and congenital heart defect. Rev Romana Med Lab. 2018;26(4):461-70. DOI: 10.2478/rrlm-2018-003210.2478/rrlm-2018-0032]Open DOISearch in Google Scholar
[6. Drugan C, Drugan T, Caillaud C, Grigorescu-Sido P, Nistor T, Crăciun AM. Laboratory diagnosis and follow-up of Romanian Gaucher disease patients. Rev Romana Med Lab. 2017;25(3):275-85. DOI: 10.1515/rrlm-2017-001810.1515/rrlm-2017-0018]Open DOISearch in Google Scholar
[7. Sabin O, Bocșan IC, Trifa A, Major ZZ, Heghes SC, Brusturean Bota E, et al. Correlation between ABCB1 gene polymorphisms, antiepileptic drug concentrations and treatment response. Rev Romana Med Lab. 2018;26(4):479-87. DOI: 10.2478/rrlm-2018-001210.2478/rrlm-2018-0012]Open DOISearch in Google Scholar
[8. Muntean I, Şuteu C, Togănel R, Bănescu C. Association between MDR1 gene polymorphism and clinical course of pediatric pulmonary arterial hypertension. Rev Romana Med Lab. 2018;26(3):305-12. DOI: 10.2478/rrlm-2018-002510.2478/rrlm-2018-0025]Search in Google Scholar
[9. Negovan A, Iancu M, Moldovan V, Pantea M, Sarkany K, Bataga S, et al. Influence of MDR1 C3435T, CYP2C19*2 and CYP2C19*3 gene polymorphisms and clinical characteristics on the severity of gastric lesions: a case-control study. J Gastrointestin Liver Dis. 2016;25(2):258-60. DOI: 10.15403/jgld.2014.1121.252.mdr.10.15403/jgld.2014.1121.252.mdr]Search in Google Scholar
[10. Georgescu AM, Bănescu C, Badea I, Moldovan V, Huțanu A, Voidăzan S, et al. IL-6 gene polymorphisms and sepsis in ICU adult Romanian patients: a prospective study. Rev Romana Med Lab. 2017;25(1):75-89. DOI: 10.1515/rrlm-2016-004410.1515/rrlm-2016-0044]Search in Google Scholar
[11. Negovan A, Iancu M, Moldovan V, Mocan S, Banescu C. The Interaction between GSTT1, GSTM1, and GSTP1 Ile105Val Gene Polymorphisms and Environmental Risk Factors in Premalignant Gastric Lesions Risk. Biomed Res Int. 2017;2017:7365080. DOI: 10.1155/2017/7365080.10.1155/2017/7365080]Open DOISearch in Google Scholar
[12. Mărginean A, Bănescu C, Moldovan V, Scridon A, Mărginean M, Bălaşa R, et al. The Impact of CYP2C19 Loss-of-Function Polymorphisms, Clinical, and Demographic Variables on Platelet Response to Clopidogrel Evaluated Using Impedance Aggregometry. Clin Appl Thromb Hemost. 2017;23(3):255-65. DOI: 10.1177/1076029616629211.10.1177/1076029616629211]Open DOISearch in Google Scholar
[13. Lazăr C, Popp R, Al-Khzouz C, Mihuț G, Grigorescu-Sido P. GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss. Rev Romana Med Lab. 2017;25(1):37-46. DOI: 10.1515/rrlm-2017-000410.1515/rrlm-2017-0004]Open DOISearch in Google Scholar
[14. Bogliş A, Tripon F, Bănescu C. The utility of molecular genetic techniques in craniosynostosis cases associated with intellectual disability. Rev Romana Med Lab. 2018;26(4):471-7. DOI: 10.2478/rrlm-2018-003310.2478/rrlm-2018-0033]Open DOISearch in Google Scholar
[15. Goidescu IG, Eniu DT, Caracostea GV, Cruciat G, Stamatian F. Associations of pathogenic mutations responsible for breast cancer risk with histology and immunohistochemistry in Romanian population. Rev Romana Med Lab. 2018;26(2):165-75. DOI: 10.1515/rrlm-2017-003710.1515/rrlm-2017-0037]Open DOISearch in Google Scholar
[16. Maier D, Florea A, Tilinca MC, Zazgyva A, Cosgarea R. NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis. Rev Romana Med Lab. 2016;24(4):387-97. DOI: 10.1515/rrlm-2016-003410.1515/rrlm-2016-0034]Open DOISearch in Google Scholar
[17. Negura L, Negura A. Sanger sequencing of MMR genes in a one-plate system. Rev Romana Med Lab. 2018;26(2):153-63. DOI: 10.2478/rrlm-2018-000810.2478/rrlm-2018-0008]Open DOISearch in Google Scholar
[18. Coriu D, Jardan D, Jardan C, Tălmaci R, Dragomir M, Coliţă A. A new assay to identify recurrent mutations in acute myeloid leukemia using next-generation sequencing. Rev Romana Med Lab. 2014;22(1):93–9. DOI: 10.2478/rrlm-2014-000310.2478/rrlm-2014-0003]Open DOISearch in Google Scholar