Pregled po CROSBI profilu: Lukrecija Brečević (CROSBI Profil: 20332, MBZ: 82115)
Pronađeno 40 radova
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26.Brecevic L; Verdorfer I; Saul W; Trautmann U; Gebhart EThe cytogenetic view of standard comparative genomic hybridization (CGH): Deletions of 20q in human leukemia as a measure of the sensitivity of the technique // Anticancer research, 21 (2001), 89-92 (podatak o recenziji nije dostupan, članak, ostalo)
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27.Gebhart, E.; Verdorfer, I.; Saul, W.; Trautmann, U.; Brečević, LukrecijaDelimiting the use of comparative genomic hybridization in human myeloid neoplastic disorders // International journal of oncology, 16 (2000), 6; 1099-1105 doi:10.3892/ijo.16.6.1099 (međunarodna recenzija, članak, znanstveni)
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28.Brečević, Lukrecija; Basaran, Seher; Dutly, Fabrizio; Rothlisberger, Benno; Schinzel, Albert.Tandem triplication of chromosome 13q14 with inverted interstitial segment in a 4 year old girl. // Journal of Medical Genetics, 37 (2000), 4; 964-967. (međunarodna recenzija, članak, znanstveni)
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29.Kotzot, D.; Martinez, M.J.; Bagci, G.; Basaran, S.; Baumer, A.; Binkert, F.; Brečević, Lukrecija; Castellan, C.; Chrzanowska, K.; Dutly, F. et al.Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications. // Journal of Medical Genetics, 37 (2000), 4; 281-286. (međunarodna recenzija, članak, znanstveni)
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30.Frascella, E.; Lenzini, E.; Schafer, B.W.; Brečević, Lukrecija; Dorigo, E.; Toffolatti, L.; Nanni, P.; De Giovanni, C.; Rosolen, A.Concomitant amplification and expression of PAX7-FKHR and MYCN in a human rhabdomyosarcoma cell line carrying a cryptic t(1 ; 13). // Cancer Genetics and Cytogenetics, 121 (2000), 2; 139-145 (međunarodna recenzija, članak, znanstveni)
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31.Utkus, A.; Sorokina, I.; Kucinskas, V.; Röthlisberger, B.; Balmer, D.; Brečević, Lukrecija; Schinzel, A.Duplication of segment 1p21 following paternal insertional translocation, ins(6 ; 1)(q25 ; p13.3p22.1) // Journal of medical genetics, 36 (1999), 1; 73-76 doi:10.1136/jmg.36.1.73 (međunarodna recenzija, članak, znanstveni)
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32.Riegel M; Castellan C; Balmer D; Brecevic L; Schinzel A.Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes // AMERICAN JOURNAL OF MEDICAL GENETICS, 82 (1999), 3; 249-253 (međunarodna recenzija, članak, znanstveni)
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33.Röthlisberger, B.; Kotzot, D.; Brečević, Lukrecija; Koehler, M.; Balmer, D.; Binkert, F.; Schinzel, A.Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes // European journal of human genetics, 7 (1999), 8; 873-883 (međunarodna recenzija, članak, znanstveni)
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34.Čekada, Senija; Kilvain, S.; Brajenović-Milić, Bojana; Brečević, Lukrecija, Kirinčić-Paučić, Ela; Franulović J.Partial trisomy 13q22-qter and monosomy 18q21-qter as a result of familial translocation // Acta Paediatrica (Oslo), 88 (1999), 6; 675-678 (međunarodna recenzija, članak, znanstveni)
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35.Fokstuen, S.; Arbenz, U.; Artan, S.; Dutly, F.; Bauersfeld, U.; Brečević, Lukrecija; Fasnacht, M.; Röthlisberger, B.; Schinzel, A.22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin // Clinical genetics, 53 (1998), 1; 63-69 (podatak o recenziji nije dostupan, članak, ostalo)
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36.Chrzanowska, KH.; Krajewska-Walasek, M.; Kuś, J.; Michałkiewicz, J.; Maziarka, D.; Wolski, J.K.; Brečević, Lukrecija; Madaliński, K.Kabuki (Niikawa-Kuroki) syndrome associated with immunodeficiency // Clinical genetics, 53 (1998), 4; 308-312 doi:10.1111/j.1399-0004.1998.tb02702.x (međunarodna recenzija, članak, znanstveni)
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37.Schinzel, A.; Braegger, C.P.; Brečević, Lukrecija; Dutly, F.; Binkert, F.Interstitial deletion, del(4)(q12q21.1), owing to de novo unbalanced translocation in a 2 year old girl: further evidence that the piebald trait maps to proximal 4q12 // Journal of medical genetics, 34 (1997), 8; 692-695 doi:10.1136/jmg.34.8.692 (međunarodna recenzija, članak, znanstveni)
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38.Schinzel, A.; Kotzot, D.; Brečević, Lukrecija; Robinson, W.P.; Dutly, F.; Dauwerse, H.; Binkert, F.; Baumer, A.; Ausserer, B.Trisomy first, translocation second, uniparental disomy and partial trisomy third: A new mechanism for complex chromosomal aneuploidy // European journal of human genetics, 5 (1997), 5; 308-314 (podatak o recenziji nije dostupan, članak, ostalo)
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39.Schinzel, A.; Brečević, Lukrecija; Dutly, F.; Baumer, A.; Binkert, F.; Largo, RH.Multiple congenital anomalies including the Rieger eye malformation in a boy with interstitial deletion of (4)(q25 -> q27) secondary to a balanced insertion in his normal father: evidence for haplotype insufficiency causing the Rieger malformation // Journal of medical genetics, 34 (1997), 8; 1012-1014 doi:10.1136/jmg.34.12.1012 (podatak o recenziji nije dostupan, članak, ostalo)
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40.Borovecki, Fran; Brecevic, Lukrecija; Gotovac Jerčić, Kristina; Rincic, MartinaGenetic diagnostics of intellectual disability disorder, autism spectrum disorder and epilepsy
