| Role of chromosomal translocations in recurrent spontaneous abortion S Farcas, V Belengeanu, C Popa, D Stoicanescu, M Stoian, M Veliscu, ... Timisoara Med J 2, 117-21, 2007 | 30 | 2007 |
| A de novo 2.3 Mb deletion in 2q24. 2q24. 3 in a 20-month-old developmentally delayed girl V Belengeanu, TH Gamage, S Farcas, M Stoian, N Andreescu, ... Gene 539 (1), 168-172, 2014 | 24 | 2014 |
| Structural chromosomal anomalies detected by prenatal genetic diagnosis: our experience S Farcaş, CD Crişan, N Andreescu, M Stoian, AG Motoc Rom J Morphol Embryol 54 (2), 377-83, 2013 | 18 | 2013 |
| Assessment of chromosomal aneuploidies in sperm of infertile males by using FISH technique NI Andreescu, M Cosma, SS Farcas, M Stoian, DG Amzar, M Puiu Rom J Morphol Embryol 57 (1), 173-178, 2016 | 15 | 2016 |
| Ichthyosis congenita, harlequin fetus type: a case report V Belengeanu, D Stoicanescu, M Stoian, N Andreescu, C Budisan Advances in Medical Sciences 54 (1), 113, 2009 | 15 | 2009 |
| Considerations regarding the implication of polymorphic variants and chromosomal inversions in recurrent miscarriage S Farcas, V Belengeanu, M Stoian, D Stoicanescu, C Popa, N Andreescu Off J Romanian Soci Pediatr Surg 10 (39-40), 7-11, 2007 | 12 | 2007 |
| The heterogeneity of craniofacial morphology in Prader-Willi patients D Belengeanu, C Bratu, M Stoian, A Motoc, E Ormerod, AC Podariu, ... Rom J Morphol Embryol 53 (3), 527-532, 2012 | 11 | 2012 |
| Analyses of numerical aberrations of chromosome 17 and tp53 gene deletion/amplification in human oral squamous cell carcinoma using dual-color fluorescence in situ hybridization N Meszaros, D Belengeanu, D Stoicănescu, N Andreescu, S Farcaş, ... Tom 17 (1), 142-6, 2010 | 6 | 2010 |
| Trisomy 8 mosaicism with atypical phenotypic features V Belengeanu, M Boia, S Farcas, C Popa, M Stoian, A Belengeanu J. Pediatr 13, 36-39, 2010 | 3 | 2010 |
| PATERN OF CEPHALOMETRIC ANALISYS AND DENTAL PROFILE IN A GIRL WITH PRADER-WILLI SINDROME D Belengeanu, C Bratu, N Andreescu, M STOIAN, AC PODARIU | 2 | 2011 |
| Unbalanced karyotype in a human foetus due to a recurrent familial translocation N Andreescu, D Stoicănescu, A Belengeanu, S Farcaş, C Popa, M Stoian, ... Analele Universităţii din Oradea-Fascicula Biologie Tom, 9-13, 2010 | 2 | 2010 |
| VARIABLE PROGNOSIS IN TRISOMY 18 (EDWARDS SYNDROME)-3 CLINICAL CASES PRESENTATION. S Farcas, V Belengeanu, M Stoian, N Andreescu, D Belengeanu, M Boia Jurnalul Pediatrului 16, 2013 | 1 | 2013 |
| Lethal evolution of a newborn with consistent features of hydrolethalus syndrome-Romanian patient V Belengeanu, H Viskari, J Tallila, J Lahtela, S Farcas, N Andreescu, ... Genetic Counseling 22 (3), 293, 2011 | 1 | 2011 |
| NIJMEGEN BREAKAGE SYNDROME CLINICO-CYTOGENETIC PATTERN E Ormerod¹, V Belengeanu, M Stoian, N Andreescu, S Farcas, C Popa, ... REVISTA SOCIETĂŢII ROMÂNE DE CHIRURGIE PEDIATRICĂ, 19, 2009 | 1 | 2009 |
| Rare association between two genetic conditions: turner syndrome and beta thalassemia minor D STOICANESCU, M CEVEI, V BELENGEANU, M STOIAN, ... Analele Univ din Oradea Fasc Biol 2016 (2), 138-41, 2009 | 1 | 2009 |
| Therapeutical perspectives in osteogenesis imperfecta D Stoicanescu, V Belengeanu, M Stoian, O Marginean, C Popoiu, M Puiu REVISTA SOCIETĂŢII ROMÂNE DE CHIRURGIE PEDIATRICĂ, 6, 2009 | 1 | 2009 |
| Trisomy 18 and agenesis of corpus callosum: A case report V Belengeanu¹, M Boia¹, G Diaconescu, N Andreescu¹, S Farcas¹, ... ISSN p 1221-7212, 3, 2007 | 1 | 2007 |
| The role of fluorescence in situ hybridization in assessing the cytogenetically diagnosis in cryptical mosaicism aneuploydies M Stoian, V Belengeanu, M Boia, N Andreescu, S Farcas Jurnalul Pediatrului 3738, 6-10, 2007 | 1 | 2007 |
| LEJEUNE SYNDROME–A MICRODELETION SYNDROME–CASE REPORT M Stoian¹, V Belengeanu¹, S Farcas¹, N Andreescu¹, C Popa¹, M Boia¹, ... REVISTA SOCIETĂŢII ROMÂNE DE CHIRURGIE PEDIATRICĂ, 16, 0 | 1 | |
| Severe dysmorphic phenotype associated with small ring chromosome 13 V Belengeanu, M Stoian, S Farcas, C Popescu, N Andreescu, ... CHROMOSOME RESEARCH 21, S40-S40, 2013 | | 2013 |
