S strokovnostjo in prijaznostjo do zdravja
MENI VSEBINA

Znanstveno-raziskovalno delo

Raziskovalni projekti

Laboratorij sodeluje v International Breakpoint Mapping Consortium od leta 2014. Mednarodni raziskovalni projekti:
  1. “Utilisation de l’Hybridation Génomique Comparative (CGH) pour le diagnostic des leucémies et des lymphomes.” (Uporaba CGH pri diagnostiki levkemij in limfomov.) Francoski partner Muleris M., Institut Curie, Paris. (2003,2004)…
  2. " Študij metilacije DNA na kromosomih pri razvoju in onkogenezi." s francoskim partnerjem ( dr.Claire Bourgeois, Inštitut Curie, Pariz) v okviru francosko-slovenskega sodelovanja  PROTEUS;  MZT;  1995,1996.
Republiški raziskovalni projekti Republiški raziskovalni program:
  1. Republiški raziskovalni program : Primerjalna genomika in genomska biodiverziteta. (P4-0220) (2003-2008, 2009-20015).
Republiški raziskovalni projekt :
  1. „Genomsko ozadje odpornosti na mastitis.“ (J4-7328) (2014-2018).
  2. » Uporaba izražanja izbranih genov kot novih potencialnih markerjev pri diagnostiki in prognozi raka prostate.« (L3-2364) (2009-2014)
  3. »Uporabnost primerjalne genomske hibridizacije (PGH) pri diagnostiki levkemij in limfomov.« (L3-4549)  (2003/04/05)
  4. »Subtelomerne kromosomske spremembe pri idiopatski mentalni zaostalosti.« MZT; 2000,2001; Šifra projekta: L3-2145.
  5. »Študij DNA metilacije na ekstraembrionalnem tkivu.« MZT; 1998,1999; Šifra projekta: J3-0062.
  6. » Uporaba metod molekularne citogenetke pri ugotavljanju kromosomskih anomalij. « MZT; 1996,1997; Šifra projekta: L3-7845.
  7. " Ugotavljanje kromosomskih nepravilnosti pri otrocih nizke rasti" v okviru projekta  " Nove metode zdravljenja za skrajšanje rehabilitacije in hospitalizacije." ( nosilec: doc.dr.JankoBerčič, dr.med.) prijavljene pri Oddelku za družbene dejavnosti Občine Maribor, 1994,1995,1996.
Interni raziskovalni projekti

  1. „Analiza genetskih dejavnikov, vpletenih v zgodnje spontane splave. „ (IRP-2012/01-01)
  2. „Analiza kandidatnih genov pri razvoju planocelularnega karcinoma ustne votline in ustnega dela žrela.“(IRP-2013/01-04)
  3. „Neinvazivno določanje anevplodije v prenatalni diagnostiki z metodo digitalne verižne reakcije s polimerazo.“ (IRP-2013/02-05)
  4. „Določanje genskih mutacij pri naglušnosti.“ (IRP-2014/01-14)
  5. „Nova generacija sekveniranja eksoma otrok s prirojenimi anomalijami, displastičnimi znaki ter duševnim in razvojnim zaostankom.“ (IRP-2015/01-07).
  6. „Analiza 174 genov povezanih z dednimi kardiološkimi stanji.“ (IRP-2016/01-02).
  7. „Uporaba metode sekvenciranja nove generacije (NGS) pri določanju patogenih različic v genih BRCA1 in BRCA2 pri bolnikih z rakom dojke ali jajčnikov in asimptomatskih posameznikih s pozitivno družinsko anamnezo.“ (IRP-2017/01-03).
  8. „Primerjava testov Xpert Bladdre Cancer Detection in UroVysion Bladder Cancer Kit pri diagnostiki prehodnoceličnega karcinoma sečnega mehurja.(IRP-2017/01-06)
  9. „Spremljanje fuzijskega onkogena ABL/BCR pri kronični mieloični levkemiji. (IRP-2017/01-05)

Publikacije objavljene v svetovni znanstveni literaturi

1. KOKALJ-VOKAČ, Nadja, SAINT-RUF, C..., LEFRANÇOIS, Danielle, VIEGAS-PÉQUIGNOT, Evani, LEMIEUX, N..., MALFOY, Bernard, DUTRILLAUX, Bernard. A t(X;15)(q23;q25) with Xq reactivation in a lymphoblastoid cell line from Fanconi anemia. Cytogenet. cell genet., 1991, 57, str. 11-15. [COBISS.SI-ID 7232776]

2. LEFRANÇOIS, Danielle, KOKALJ-VOKAČ, Nadja, VIEGAS-PÉQUIGNOT, Evani, MONTAGNIER, Luc, DUTRILLAUX, Bernard. High recurrence of rearrangements involving chromosome 14 in an ataxia telangiectasia lymphoblastoid cell line and its mutagen-treated derivatives. Hum Genet, 1991, 86, str. 475-480, ilustr. [COBISS.SI-ID 7233032]

3. KOKALJ-VOKAČ, Nadja, ALMEIDA, Anna, VIEGAS-PEQUIGNOT, E..., JEANPIERRE, M..., MALFOY, Bernard, DUTRILLAUX, Bernard. Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin. Cytogenet. cell genet., 1993, 63, št. 1, str. 11-15. [COBISS.SI-ID 90329]

4. KOKALJ-VOKAČ, Nadja, ALEMEIDA, Anna, GERBAULT-SEUREAU, Michele, MALFOY, Bernard, DUTRILLAUX, Bernard. Two-color FISH characterization of i(1q) and der(1;16) in human breast cancer cells. Genes chromosomes cancer, 1993, 7, št. 1, str. 8-14. [COBISS.SI-ID 90073]

5. ALMEIDA, Anna, KOKALJ-VOKAČ, Nadja, LEFRANCOIS, Danielle, VIEGAS-PÉQUIGNOT, E..., JEANPIERRE, M..., DUTRILLAUX, Bernard, MALFOY, Bernard. Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines. Hum Genet, 1993, 91, št. 6, str. 538-546. [COBISS.SI-ID 89561]

6. BOURGEOIS, C.A..., KOKALJ-VOKAČ, Nadja, DUTRILLAUX, A.M..., POISSON, M..., DELATTRE, J.Y..., VEGA, F..., MALFOY, Bernard, DUTRILLAUX, Bernard. Caracterisation par hybridation in situ des remaniements chromosomiques dans un glioblastome. Bull. Cancer, 1994, let. 81, str. 360-365. [COBISS.SI-ID 90585]

7. MONTPELLIER, Claire, BOURGEOIS, Claire A., KOKALJ-VOKAČ, Nadja, MULERIS, Martine, NIVELEAU, Alain, REYNAUD, Cecile, GIBAUD, Anne, MALFOY, Bernard, DUTRILLAUX, Bernard. Detection of methylcytosine-rich heterochromatin on banded chromosomes : Application to cells with various status of DNA methylation. Cancer genet. cytogenet.. [Print ed.], 1994, 78, št. 1, str. 87-93. [COBISS.SI-ID 134873]

8. BARBIN, A..., MONTPELLIER, Claire, KOKALJ-VOKAČ, Nadja, GIBAUD, Anne, NIVELEAU, Alain, MALFOY, Bernard, DUTRILLAUX, Bernard, BOURGEOIS, Claire A. New sites of methylcytosine-rich DNA detected on metaphase chromosomes. Hum Genet, 1994, 94, št. 6, str. 684-692. [COBISS.SI-ID 89817]

9. ZAGRADIŠNIK, Boris, ZIDAR, Janez, MEZNARIČ-PETRUŠA, Mija, ŽUPANČIČ, Neža, PETERLIN, Borut. The use of quantitative PCR for the detection of DMD/BMD carriers and duplications in the dystrophin gene. Acta cardiomiol., 1996, let. 8, str. 93-98. [COBISS.SI-ID 7054553]

10. KOKALJ-VOKAČ, Nadja, ZAGORAC, Andreja, PRISTOVNIK, Marija, BOURGEOIS, Claire A., DUTRILLAUX, Bernard. DNA methylation of the extraembryonic tissues : an in situ study on human metaphase chromosomes. Chomosom. res., 1998, letn. 6, št. 3, str. 161-166. [COBISS.SI-ID 10753241]

11. KOKALJ-VOKAČ, Nadja, MEDICA, Igor, ZAGORAC, Andreja, ZAGRADIŠNIK, Boris, ERJAVEC, Alenka, GREGORIČ, Alojz. A case of insertional translocation resulting in partial trisomy 16p. Ann. génét. (Paris). [Print ed.], 2000, 43, str. 131-135, ilustr. [COBISS.SI-ID 10611720]

12. KOKALJ-VOKAČ, Nadja, SEME-CIGLENEČKI, Polona, ERJAVEC, Alenka, ZAGRADIŠNIK, Boris, ZAGORAC, Andreja. Partial Xp duplication in a girl with dysmorphic features : the change in replication pattern of late-replicating dupX chromosome : short report. Clin. genet., Jan. 2002, vol. 61, no. 1, str. 54-61. [COBISS.SI-ID 890431]

13. MARČUN-VARDA, Nataša, KOKALJ-VOKAČ, Nadja, KANIČ, Zlatka, BRAČIČ, Katarina, ERJAVEC, Alenka, ZAGRADIŠNIK, Boris, GREGORIČ, Alojz. Early renal insufficiency in a neonate with de novo partial trisomy of chromosome 10q. Am. j. med. genet., 2003, vol. 123A, no. 2, str. 164-168. [COBISS.SI-ID 1385279]

14. ZVER, Samo, KOKALJ-VOKAČ, Nadja, ZAGRADIŠNIK, Boris, ERJAVEC, Alenka, ZAGORAC, Andreja, PRELOŽNIK-ZUPAN, Irena, ČERNELČ, Peter. T cell prolymphocytic leukemia with new chromosome rearrangements. Acta Haematol., 2004, vol. 111, no. 3, str. 168-170. [COBISS.SI-ID 1624127]

15. ZAGRADIŠNIK, Boris, BRAČIČ, Katarina, MARČUN-VARDA, Nataša, KOKALJ-VOKAČ, Nadja, GREGORIČ, Alojz. G-protein ß3 subunit gene C825T polymorphism in patients with vesico-ureteric reflux. Ann. génét. (Paris). [Print ed.], 2004, vol. 47, no. 3, str. 209-216. [COBISS.SI-ID 1674303]

16. HAJDINJAK, Tine, ZAGRADIŠNIK, Boris. Prostate cancer and polymorphism D85Y in gene for dihydrotestosterone degrading enzyme UGT2B15 : frequency of DD homozygotes increases with gleason score. Prostate, 2004, vol. 59, no. 4, str. 436-439. [COBISS.SI-ID 1605695]

17. Danish nation-wide cohort [and collaborators], KOKALJ-VOKAČ, Nadja. An excess of chromosome 1 breakpoints in male infertility. Eur J Hum Genet, 2004, vol. 12, no. 12, str. 993-1000. [COBISS.SI-ID 1770047]

18. KOKALJ-VOKAČ, Nadja, MARČUN-VARDA, Nataša, ZAGORAC, Andreja, ERJAVEC, Alenka, ZAGRADIŠNIK, Boris, TODOROVIČ-GUID, Mirjana, GREGORIČ, Alojz. Subterminal deletion/duplication event in an affected male due to maternal X chromosome pericentric inversion. Eur J Pediatr, 2004, vol. 163, no. 11, str. 658-663. [COBISS.SI-ID 1710655]

19. LENASI, Tina, KOKALJ-VOKAČ, Nadja, NARAT, Mojca, BALDI, Antonella, DOVČ, Peter. Functional study of the equine ß-casein and K-casein gene promoters. J. Dairy Res., 2005, letn. 72, spec. Iss., str. 34-43. [COBISS.SI-ID 1759624]

20. GREGORIČ, Alojz, RABELINK, Gwenda M., KOKALJ-VOKAČ, Nadja, MARČUN-VARDA, Nataša, ZAGRADIŠNIK, Boris. Eighteen-year follow-up of a patient with partial hypoxanthine phosphoribosyltransferase deficiency and a new mutation. Pediatr Nephrol (Berl. West), 2005, vol. 20, no. 9, str. 1346-1348. [COBISS.SI-ID 2047039]

21. MARČUN-VARDA, Nataša, ZAGRADIŠNIK, Boris, STANGLER HERODEŽ, Špela, KOKALJ-VOKAČ, Nadja, GREGORIČ, Alojz. Polymorphisms in four candidate genes in young patients with essential hypertension. Acta Paediatr, 2006, vol. 95, no. 3, str. 353-358. [COBISS.SI-ID

22. ERJAVEC ŠKERGET, Alenka, STANGLER HERODEŽ, Špela, ZAGORAC, Andreja, ZAGRADIŠNIK, Boris, KOKALJ-VOKAČ, Nadja. Subtelomeric chromosome rearrangements in children with idiopathic mental retardation: applicability of three molecular-cytogenetic methods. Croat. med. j., 2006, vol. 47, no. 6, str. 841-850. [COBISS.SI-ID 2553151]

24. VLAISAVLJEVIĆ, Veljko, KRIŽANČIĆ BOMBEK, Lidija, KOKALJ-VOKAČ, Nadja, KOVAČIČ, Borut, ČIŽEK-SAJKO, Mojca. How safe is germinal vesicle stage oocyte rescue? Aneuploidy analysis of in vitro matured oocytes. Eur J Obstet Gynecol Reprod Biol. [Print ed.], 2007, vol. 134, no. 2, str. 213-219. [COBISS.SI-ID 2739263]

25. HAJDINJAK, Tine, KOKALJ-VOKAČ, Nadja. Re: Mecedes Marín-Aguilera, Lourdes Mengual, María José Ribal et al. Utility of fluorescence in situ hybridization as a non-invasive technique in the diagnosis of upper urinary tract urothelial carcinoma. Eur Urol 2007;51:409-15 and Alan M. Nieder, Mark S. Soloway and Harry W. Herr. Should we abandon the FISH test? Eur Urol 2007;51:1469-71. Eur. urol., 2007, vol. 52, no. 1, str. 288-289. [COBISS.SI-ID 2710847]

26. CRUCIANI, Fulvio, LA FRATTA, Roberta, TROMBETTA, Beniamino, SANTOLAMAZZA, Piero, SELLITTO, Daniele, BERAUD COLOMB, Eliane, DUGOUJON, Jean-Michel, CRIVELLARO, Federica, BENINCASA, Tamara, PASCONE, Roberto, MORAL, Pedro, WATSON, Elizabeth, MELEGH, Bela, BARBUJANI, Guido, FUSELLI, Silvia, VONA, Giuseppe, ZAGRADIŠNIK, Boris, ASSUM, Guenter, BRDICKA, Radim, KOZLOV, Andrey I., EFREMOV, Georgi, COPPA, Alfredo, NOVELLETO, Andrea, SCOZZARI, Rosaria. Tracing past human male movements in northern/eastern Africa and western Eurasia: new clues from Y-chromosomal haplogroups E-M78 and J-M12. Molecular biology and evolution, 2007, vol. 24, no. 6, str. 1300-1311. [COBISS.SI-ID 2871103]

27. ROZMAN, Tamara, DOVČ, Peter, MARIĆ, Saša, KOKALJ-VOKAČ, Nadja, ERJAVEC ŠKERGET, Alenka, RAB, P., SNOJ, Aleš. Evidence for two transferrin loci in the Salmo trutta genome. Anim. genet., 2008, vol. 39, no. 6, str. 577-585, doi: 10.1111/j.1365-2052.2008.01768.x. [COBISS.SI-ID 2376584]

28. KOKALJ-VOKAČ, Nadja, ZAGORAC, Andreja, ERJAVEC ŠKERGET, Alenka, ROŠKAR, Zlatko, PODGORNIK, Helena, ČERNELČ, Peter. Der(1;16)(q10;p10) in acute myeloid leukemia : the first female case described. Acta haematol. (Online), 2008, letn. 119, št. 1, str. 54-56, doi: 10.1159/000115965. [COBISS.SI-ID 24117977]

29. KOKALJ-VOKAČ, Nadja, KODRIČ, Tatjana, ERJAVEC ŠKERGET, Alenka, ZAGORAC, Andreja, TAKAČ, Iztok. Screening of TERC gene amplification as an additional genetic diagnostic test in detection of cervical preneoplastic lesions. Cancer genet. cytogenet.. [Print ed.], 2009, vol. 195, no. 1, str. 19-22. [COBISS.SI-ID 3500607]

30. TAKAČ, Iztok, ARKO, Darja, KODRIČ, Tatjana, POLJAK, Mario, ZAGORAC, Andreja, ERJAVEC ŠKERGET, Alenka, KOKALJ-VOKAČ, Nadja. Human telomerase gene amplification and high-risk human papillomavirus infection in women with cervical intra-epithelial neoplasia. J. int. med. res., 2009, vol. 37, no. 5, str. 1588-1595. http://www.jimronline.net/content/full/2009/93/1251.pdf. [COBISS.SI-ID 3455295]

31. STANGLER HERODEŽ, Špela, ZAGRADIŠNIK, Boris, ERJAVEC ŠKERGET, Alenka, ZAGORAC, Andreja, KOKALJ-VOKAČ, Nadja. Molecular diagnosis of PMP22 gene duplications and deletions: comparison of different methods. J. int. med. res., 2009, vol. 37, no. 5, str. 1626-1631. http://www.jimronline.net/content/full/2009/93/1246.pdf. [COBISS.SI-ID 3439935]

32. ŽERJAVIČ, Katja, ZAGRADIŠNIK, Boris, STANGLER HERODEŽ, Špela, LOKAR, Lidija, GLASER, Marjana, KOKALJ-VOKAČ, Nadja. Is the YAK2 V617F mutation a hellmark for a different forms of thrombosis?. Acta Haematol., 2010, vol. 124, no. 1, str. 49-56, doi: 10.1159/000314645. [COBISS.SI-ID 3691839]

33. CRUCIANI, Fulvio, TROMBETTA, Beniamino, ANTONELLI, Cheyenne, PASCONE, Roberto, VALESINI, Guido, SCALZI, Valentina, VONA, Giuseppe, MELEGH, Bela, ZAGRADIŠNIK, Boris, ASSUM, Guenter, EFREMOV, Georgi, SELLITTO, Daniele, SCOZZARI, Rosaria. Strong intra- and inter-continental differentiation revealed by Y chromosome SNPs M269, U106 and U152. Forensic science international, Genetics, 2010, 1 PDF datoteka (str. 1-4), doi: 10.1016/j.fsigen.2010.07.006. [COBISS.SI-ID 3699007],

34. HAJDINJAK, Tine, ZAGORAC, Andreja, ERJAVEC ŠKERGET, Alenka, KAVALAR, Rajko, KOKALJ-VOKAČ, Nadja. Fluorescentna in situ hibridizacija kot neinvazivna tehnika odkrivanja raka mehurja v vzorcih urina = Non-invasive bladder cancer detection by fluorescent in situ hybridization on urine samples. Acta medico-biotechnica, 2010, vol. 3, no. 1, str. 35-40.

35. KRGOVIĆ, Danijela, MARČUN-VARDA, Nataša, ZAGORAC, Andreja, KOKALJ-VOKAČ, Nadja. Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report. Molecular cytogenetics. [Online ed.], 2011, [Vol.] 4, 17. http://www.molecularcytogenetics.org/content/pdf/1755-8166-4-17.pdf, doi: doi:10.1186/1755-8166-4-17. [COBISS.SI-ID 4029247]

36. CRUCIANI, Fulvio, TROMBETTA, Beniamino, ANTONELLI, Cheyenne, PASCONE, Roberto, VALESINI, Guido, SCALZI, Valentina, VONA, Giuseppe, MELEGH, Bela, ZAGRADIŠNIK, Boris, ASSUM, Guenter, EFREMOV, Georgi, SELLITTO, Daniele, SCOZZARI, Rosaria. Strong intra- and inter-continental differentiation revealed by Y chromosome SNPs M269, U106 and U152. Forensic science international, Genetics, 2011, vol. 5, no. 3, str. e49-e52, doi: 10.1016/j.fsigen.2010.07.006. [COBISS.SI-ID 3699007]

37. VRŠIČ, Stanko, IVANČIČ, Anton, ŠUŠEK, Andrej, ZAGRADIŠNIK, Boris, VALDHUBER, Janez, ŠIŠKO, Metka. The World's oldest living grapevine specimen and its genetic relationships. Vitis, 2011, letn. 50, št. 4, str. 167-171. [COBISS.SI-ID 3206956].

38. ERJAVEC ŠKERGET, Alenka, STANGLER HERODEŽ, Špela, ZAGORAC, Andreja, ZAGRADIŠNIK, Boris, KOKALJ-VOKAČ, Nadja. Uporaba primerjalne genomske hibridizacije kot diagnostične metode v medicinskem genetskem laboratoriju : prva uporaba na različnih kliničnih vzorcih = The use of comparative genomic hybridization as a diagnostic tool in medical genetics laboratories : first application on different clinical samples. Acta medico-biotechnica, 2011, vol. 4, no. 1, str. 49-56. [COBISS.SI-ID 512122168]               

39. ZAGRADIŠNIK, Boris, STANGLER HERODEŽ, Špela, ERJAVEC ŠKERGET, Alenka, ZAGORAC, Andreja, KOKALJ-VOKAČ, Nadja. Detection of aneuploidy using multiplex ligation-dependent probe amplification in fetal tissues from aborted pregnancies = Določanje anevploidij z metodo pomnoževanja od ligacije odvisnih prob v fetalnih tkivih splavkov. Acta medico-biotechnica, 2011, vol. 4, no. 2, str. 51-60. [COBISS.SI-ID 4160831]   

40. KUNČNIK, Vesna, ERJAVEC ŠKERGET, Alenka, STANGLER HERODEŽ, Špela, ZAGRADIŠNIK, Boris, KOKALJ-VOKAČ, Nadja. Odkrivanje sindroma fragilnega kromosoma X na osnovi tehnologije PCR pri moški populaciji iz severovzhodne Slovenije = Detection of fragile X syndrome based on PCR technology in the male population of north-eastern Slovenia. Slov. pediatr., 2012, letn. 19, št. 1, str. 26-34. [COBISS.SI-ID 4271423]

41.ŽERJAVIČ, Katja, ZAGRADIŠNIK, Boris, LOKAR, Lidija, GLASER, Marjana, KOKALJ-VOKAČ, Nadja. The association of the JAK2 46/1 haplotype with non-splanchnic venous thrombosis. Thrombosis research, ISSN 0049-3848. [Print ed.], 2013, vol. , no. , str. http://www.sciencedirect.com/science/article/pii/S0049384813002727, doi: 10.1016/j.thromres.2013.06.021. [COBISS.SI-ID 4724799], [JCR, SNIP, WoS do 7. 10. 2013: št. citatov (TC): 0, čistih citatov (CI): 0, normirano št. čistih citatov (NC): 0, Scopus do 21. 9. 2013: št. citatov (TC): 0, čistih citatov (CI): 0, normirano št. čistih citatov (NC): 0]

42. MACEDONI-LUKŠIČ, Marta, KRGOVIĆ, Danijela, ZAGRADIŠNIK, Boris, KOKALJ-VOKAČ, Nadja. Deletion of the last exon of SHANK3 gene produces the full Phelan-McDermid phenotype : a case report. Gene, ISSN 0378-1119. [Print ed.], 2013, vol. 524, no. 2, str. 386-389, ilustr. http://www.sciencedirect.com/science/article/pii/S0378111913004642, doi: 10.1016/j.gene.2013.03.141. [COBISS.SI-ID 721836], [JCR, SNIP, WoS do 16. 9. 2013: št. citatov (TC): 0, čistih citatov (CI): 0, normirano št. čistih citatov (NC): 0, Scopus do 15. 6. 2013: št. citatov (TC): 0, čistih citatov (CI): 0, normirano št. čistih citatov (NC): 0]

43. ERJAVEC ŠKERGET, Alenka, STANGLER HERODEŽ, Špela, ZAGORAC, Andreja, ZAGRADIŠNIK, Boris, MUJEZINOVIĆ, Faris, KOKALJ-VOKAČ, Nadja. Slovenian five-year experiences with rapid prenatal diagnosis of common chromosome aneuploidies using quantitative fluorescence polymerase chain reaction. Genetic testing and molecular biomarkers, ISSN 1945-0265, 2013, vol. , no. , str. http://online.liebertpub.com/doi/abs/10.1089/gtmb.2013.0082, doi: 10.1089/gtmb.2013.0082. [COBISS.SI-ID 4738623], [JCR, SNIP, WoS do 7. 10. 2013: št. citatov (TC): 0, čistih citatov (CI): 0, normirano št. čistih citatov (NC): 0, Scopus do 23. 9. 2013: št. citatov (TC): 0, čistih citatov (CI): 0, normirano št. čistih citatov (NC): 0]

44. TODOROVIČ-GUID, Mirjana, KOKALJ-VOKAČ, Nadja, MARČUN-VARDA, Nataša. A girl with an asymptomatic parietal encephalocele. Paediatria Croatica, ISSN 1330-1403, 2013, vol. 57, no. 1, str. 83-86, ilustr. [COBISS.SI-ID 4590143], [JCR, SNIP, Scopus do 9. 7. 2013: št. citatov (TC): 0, čistih citatov (CI): 0, normirano št. čistih citatov (NC): 0]

45. STANGLER HERODEŽ, Špela, ZAGRADIŠNIK, Boris, ERJAVEC ŠKERGET, Alenka, ZAGORAC, Andreja, TAKAČ, Iztok, VLAISAVLJEVIĆ, Veljko, LOKAR, Lidija, KOKALJ-VOKAČ, Nadja. MTHFR C677T and A1298C genotypes and haplotypes in Slovenian couples with unexplained infertility problems and in embryonic tissues from spontaneous abortions. BJMG, ISSN 1311-0160, 2013, vol. 16, [no.] 1, str. 31-39. http://www.bjmg.edu.mk/record.asp?recordid=633. [COBISS.SI-ID 4757823], [JCR, SNIP]

46. STANGLER HERODEŽ, Špela, STANKOVIČ, Nastja, ZAGRADIŠNIK, Boris, ERJAVEC ŠKERGET, Alenka, KOKALJ-VOKAČ, Nadja. Detection of vkorc1 polymorphism : comparison of polymerase chain reaction/restriction fragment length polymorphism (pcr + rflp) with allelespecific polymerase chain reaction = Ugotavljanje VKORC1 polimorfizma : primerjava metod verižne reakcije s polimerazo/polimorfizma dolžin restrikcijskih fragmentov (PCR + RFLP) z alelno specifično verižno reakcijo s polimerazo. Acta medico-biotechnica, ISSN 1855-5640, 2013, vol. 6, no. 2, str. 47-52, ilustr. http://www.actamedbio.mf.uni-mb.si/05_11id_amb_69_12.pdf. [COBISS.SI-ID 4863039]

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