Pregled po CROSBI profilu: Leona Morožin Pohovski (CROSBI Profil: 22012, MBZ: 261772)
Pronađeno 47 radova
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1.Vulin, Katarina; Odak, Ljubica; Morožin Pohovski, Leona; Đaković, Ivana; Tripalo Batoš, Ana; Meašić, Ana-Maria; Kero, Mijana; Sansović, Ivona; Bobinec, Adrana; Barišić, IngeborgChromosomal microarray in clinical diagnosis of cerebral palsy // Journal of Bioanthropology ; vol.2, no.1, 2022. Program and abstracts: The Twelfth ISABS Conference on Forensic and Anthropological Genetics and Mayo Clinic Lectures in Individualized Medicine ; June 22-27, 2022, Dubrovnik, Croatia. / Marjanović, D (ur.).
Zagreb: Institut za antropologiju, 2022. str. 308-308 doi:10.54062/jb (predavanje, međunarodna recenzija, sažetak, znanstveni) -
2.Morozin Pohovski, Leona; Bobinec, Adriana; Measic, Ana-Maria; Sansovic, Ivona; Barisic, IngeborgA new case of intragenic deletion of the TCF4 gene without features of Pitt-Hopkins syndrome // Molecular and experimental biology in medicine, 3 (2020), 2; 56-58 doi:10.33602/mebm.3.2.8 (recenziran, članak, stručni)
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3.Morožin Pohovski, Leona; Barišić, IngeborgMultiplex ligation-dependent probe amplification (MLPA) genetic testing in the diagnostics of children with developmental delay/intellectual disabilities. // Folia medica Facultatis medicinae Universitatis Saraeviensis, 49 (2014), 1; 15-21 (podatak o recenziji nije dostupan, pregledni rad, ostalo)
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4.Kero, Mijana; Morožin-Pohovski, Leona; Čače, Neven; Barišić, IngeborgSindrom Kleefstra: prikaz bolesnika s asimetričnom hipetrofičnom kardiomiopatijom // Pediatria Croatica Supplement
Dubrovnik, Hrvatska, 2014. str. 106-107 (poster, domaća recenzija, sažetak, znanstveni) -
5.Morožin Pohovski, Leona; Barišić, Ingeborg; Riegel, Mariluce; Schinzel, AlbertMolekularna karakterizacija prstenastog kromosoma 9 primjenom tehnike komparativne genomske hibridizacije na mikropostroju // Pediatria Croatica Supplement
Dubrovnik, Hrvatska, 2014. (poster, domaća recenzija, sažetak, znanstveni) -
6.Morožin Pohovski, L; Barišić, IIdentification of microdeletion 8q23.3q24.11 by MLPA in patient with multiple hereditary exostoses // European journal of human genetics Supplement 1
Milano, Italija: Nature Publishing Group, 2014. str. 447-448 (poster, međunarodna recenzija, sažetak, znanstveni) -
7.Sansović, I; Morožin Pohovski, L; Barišić, IMicroduplication of Xp22.31 region involving the STS gene in two males with intellectual disability // European journal of human genetics
Milano, Italija: Nature Publishing Group, 2014. str. 163-164 (poster, međunarodna recenzija, sažetak, znanstveni) -
8.Morožin-Pohovski, L; Barišić, I:Multiple ligation-dependent proble amplification (MLPA) genetic testing in the diagnostics of children with developmental delay/intellectual disabilities // Folia Medica Facultatis Medicinae Universitatis Saraeviensis
Sarajevo, 2014. str. 15-21 (predavanje, cjeloviti rad (in extenso), ostalo) -
9.Zergollern-Čupak, Ljiljana; Barišić, Ingeborg; Morožin-Pohovski, LeonaDevelopment of genetics in the world and in Croatia – forty years of the Croatian Society of Human Genetics of the Croatian Medical Association // Collegium antropologicum, 38 (2014), 3; 809-818 (podatak o recenziji nije dostupan, ostalo)
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10.Sansović, Ivona; Morožin Pohovski, Leona; Barišić, IngeborgMicroduplication of Xp22.31 region involving the STS gene in two males with intellectual disability // European Journal of Human Genetics, Volume 22, Supplement 1, May 2014 / G-J B van Ommen (ur.).
Milano, Italija: Nature Publishing Group, 2014. str. 163-164 (poster, međunarodna recenzija, sažetak, znanstveni) -
11.Odak, Ljubica; Morožin-Pohovski, Leona; Barišić, IngeborgMikrodelecija 17q21.31- prikaz dvaju bolesnika // Paediatria Croatica, 57 (2013), 1; 45-48 (recenziran, članak, stručni)
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12.Barišić, Ingeborg; Morožin Pohovski, LeonaNovi mikrodelecijski sindromi // Paediatria Croatica, 57 (2013), 4; 400-407 (recenziran, članak, stručni)
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13.Morožin Pohovski; Leona; Barišić, IngeborgMicrodeletion syndromes: copy number aberrations in patients with developmental delay/intellectual disability detected by MLPA // Chromosome Research. Supplement 1
Dublin, Irska, 2013. str. 66-67 (poster, međunarodna recenzija, sažetak, ostalo) -
14.Morožin Pohovski, Leona; Barišić, IngeborgDetection of subtelomeric copy number aberrations in patients with developmental delay/intellectual disability by MLPA // The Eighth ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine, Book of Abstracts
Split, Hrvatska, 2013. str. 290-290 (poster, međunarodna recenzija, sažetak, ostalo) -
15.Morožin Pohovski, LeonaMeđunarodni sustav nomenklature u humanoj citogenetici – ISCN 2013 // Paediatria Croatica, 57 (2013), 4; 387-391 (recenziran, članak, stručni)
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16.Morožin Pohovski, Leona; Barišić, IngeborgProbir mikrodelecijskih/mikroduplikacijskih sindroma tehnikom višestrukog umnožavanja vezanih sondi (MLPA) // Paediatria Croatica
Zagreb, Hrvatska, 2013. str. 301-301 (predavanje, domaća recenzija, sažetak, ostalo) -
17.Kero, Mijana; Morožin Pohovski, Leona; Sansović, Ivona; Odak, Ljubica; Dumić, Katja; Barišić, IngeborgCongenital anomalies in patients with submicroscopic chromosome abnormalities // Book of abstracts of 12th European Symposium on Congenital Anomalies
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 69-69 (poster, međunarodna recenzija, sažetak, ostalo) -
18.Morožin-Pohovski, Leona; Dumić Kubat, Katja, Odak, Ljubica; Barišić, IngeborgMultiplex ligation-dependent probe amplification workflow for the detection of submicroscopic chromosomal abnormalities in patients with developmental delay/intellectual disability // Molecular cytogenetics, 6 (2013), 1; 7-7 (međunarodna recenzija, članak, znanstveni)
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19.Morožin Pohovski, Leona; Barišić, IngeborgMLPA as screening method in detection of submicroscopic rearrangements detected in patients with developmental delay/intellectual disability // European Journal of Human Genetics
Nürnberg, Njemačka: Nature Publishing Group, 2012. str. 123-123 (poster, međunarodna recenzija, sažetak, ostalo) -
20.Barišić, Ingeborg; Dumić Kubat, Katja; Morožin Pohovski, Leona; Petković, Iskra; Riegel M, Schinzel, AlbertArray CGH characterisation of ring chromosome 9 formation due to inverted duplication and terminal deletion in a patient with sex- reversal // European Journal of Human Genetics
Nürnberg, Njemačka, 2012. str. 127-127 (poster, međunarodna recenzija, sažetak, ostalo) -
21.Morožin Pohovski, Leona; Barišić, IngeborgProbir aberacija subtelomera i mikrodelecijskih sindroma u bolesnika s razvojnim /intelektualnim smetnjama metodom MLPA // Paediatria Croatica, 56 (2012), 2; 18-21 (međunarodna recenzija, članak, znanstveni)
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22.Morožin Pohovski, LeonaProbir aberantnih subtelomera u dijagnostici razvojnog zaostajanja/mentalne retardacije primjenom metode višestrukog umnožavanja vezanih sondi (MLPA), 2011., doktorska disertacija, Prirodoslovno-matematički fakultet, Biološki odsjek, Zagreb
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23.Morožin Pohovski, Leona; Barišić, IngeborgScreening of patients with mental retardation using subtelomeric MLPA assay // 7th ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine Book of Abstracts
Zagreb: SABS – International Society for Applied Biological Sciences, 2011. str. 258-258 (predavanje, međunarodna recenzija, sažetak, stručni) -
24.Dumić, Katja; Morožin-Pohovski, Leona; Barišić, IngeborgDuplication of pseudoautosomal region 1 and SHOX gene could be linked with characteristic phenotype // Europan Journal of Human Genetics. Supplement 2
Amsterdam: Nature Publishing Group, 2011. str. 121-121 (poster, međunarodna recenzija, sažetak, ostalo) -
25.Odak, Ljubica; Barišić, Ingeborg; Morožin Pohovski, Leona; Riegel, Mariluce; Schinzel, AlbertA novel de novo dir dup (16) (q12.1-q21) in a girl with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case report and review of the literature // 7th ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine Book of Abstracts
Zagreb: ISABS – International Society for Applied Biological Sciences, 2011. str. 295-295 (poster, međunarodna recenzija, sažetak, stručni) -
26.Odak, Ljubica; Barišić, Ingeborg; Morožin Pohovski, Leona; Sansović, Ivona; Dumić, Katja; Jakušić, Nenad; Klobučar, Aleksandra; Grgurić, JosipDiagnostic algorithm for children with autism // 7th ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine Book of Abstracts
Zagreb: ISABS – International Society for Applied Biological Sciences, 2011. str. 261-261 (predavanje, međunarodna recenzija, sažetak, stručni) -
27.Odak, Ljubica; Barišić, Ingeborg; Morožin Pohovski, Leona; Riegl, M.; Schinzel, AlbertNovel duplication on chromosome 16 (q12.1-q21) associated with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case report // Croatian Medical Journal, 52 (2011), 3; 415-422 doi:10.3325/cmj.2011.52.415 (podatak o recenziji nije dostupan, prikaz, znanstveni)
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28.Dumić, Katja; Morožin Pohovski, Leona; Barišić, IngeborgKlinička i molekularna analiza nasljedne duplikacije gena SHOX i evolucijski očuvane sekvence u SHOX3' regiji // Paediatria Croatica. Supplement 2. / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 80-80 (poster, domaća recenzija, sažetak, znanstveni) -
29.Morožin Pohovski, Leona; Ciglar, Željka; Barišić, IngeborgDe novo mikrodelecija 4p16.3 u bolesnice s blagim fenotipom // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb: Denona, 2010. str. 81-81 (poster, domaća recenzija, sažetak, znanstveni) -
30.Odak, Ljubica; Barišić, Ingeborg; Loane, M; Bianchi, F; Calzolari, EPrenatal ultrasound diangosis of genetic syndromes. // 10th European Symposium on Prevention of Congenital Anomalies, Book of Abstracts
Bilbao, 2009. str. 62-62 (poster, međunarodna recenzija, sažetak, znanstveni) -
31.Morožin Pohovski, Leona; Sansović, Ivona; Barišić, IngeborgEvaluation of subtelomere imbalance in patients with mental retardation detected by MLPA screening // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 71-71 (poster, međunarodna recenzija, sažetak, ostalo) -
32.Morožin Pohovski, Leona; Barišić, IngeborgMolecular characterization of two patients with 9p-deletion // Paediatria Croatica. Supplement 2 / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 32-32 (poster, međunarodna recenzija, sažetak, znanstveni) -
33.Morožin Pohovski, Leona; Sansović, Ivona; Barišić, Ingeborg; Petković, IskraClinical, cytogenetic and molecular characterization of ring chromosome 9 formation due to inverted duplication and terminal deletion // European Journal of Human Genetics. Supplement 2
Beč, Austrija: Nature Publishing Group, 2009. str. 130-131 (poster, međunarodna recenzija, sažetak, znanstveni) -
34.Barišić, Ingeborg; Morožin Pohovski, Leona; Petković, Iskra; Cvetko, Željko; Stipančić, Gordana; Bagatin, MarijoScreening of Patients at Risk for 22q11 Deletion // Collegium antropologicum, 32 (2008), 1; 165-169 (recenziran, članak, znanstveni)
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35.Morožin Pohovski, Leona; Sansović, Ivona; Barišić, IngeborgMLPA as a screening method for the detection of cryptic subtelomeric rearrangements in patients with idiopathic mental retardation // European Journal of Human Genetics. Supplement 2
Barcelona, Španjolska: Nature Publishing Group, 2008. str. 123-123 (poster, međunarodna recenzija, sažetak, ostalo) -
36.Barišić, Ingeborg; Morožin Pohovski, Leona; Petković, Iskra; Cvetko, Željko; Stipančić, Gordana; Bagatin, MarioScreening of patients at risk for 22q11.2 deletion // Collegium Antropologicum, 32 (2008), 1; 165-169 (međunarodna recenzija, članak, znanstveni)
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37.Morožin-Pohovski, Leona; Sansović, Ivona; Barišić, Ingeborg;Trisomija 12p i delecija 5p: sličnost kliničkog fenotipa // Paediatria Croatica / Barišić, Ingeborg (ur.).
Zagreb, 2007. (poster, domaća recenzija, sažetak, znanstveni) -
38.Morožin Pohovski, Leona; Barišić, Ingeborg; Sansović, Ivona; Petković, IskraPartial trisomy 12p and deletion 5p: an overlap of dysmorphic features // European Journal of Human Genetics / van Ommen, Gert-Jan B. (ur.).
Leiden: Nature Publishing Group, 2007. (poster, međunarodna recenzija, sažetak, znanstveni) -
39.Morožin Pohovski, Leona; Barišić, IngeborgParcijalna delecija 5p i trisomija 12p: prikaz bolesnika // Paediatria Croatica, 50 (2006), suppl 2. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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40.Morožin-Pohovski, Leona; Petković, Iskra; Barišić, IngeborgPartial monosomy 18p : cytogenetic and clinical presentation in four patients // The fourth European-American school in forensic genetics and Mayo Clinic course in advanced molecular and cellular medicine - final program and abstracts
Dubrovnik, 2005. str. 139-139 (poster, sažetak, znanstveni) -
41.Barišić, Ingeborg; Morožin-Pohovski, Leona; Petković, IskraMajor congenital malformations and 22q11.2 microdeletion // Book of Abstracts of the 8th European Symposium on Prevention of Congenital Anomalies ; u: Archives of Perinatal Medicine. Supplement (2005) (S)
Poznań, Poljska, 2005. str. 19-19 (poster, međunarodna recenzija, sažetak, znanstveni) -
42.Barišić, Ingeborg; Petković, Iskra; Morožin-Pohovski, Leona; Cvetko, Željko; Stipančić, Gordana; Bagatin, Mario22q11.2 deletion in a series of paediatric at risk patients // Abstracts of the ..... ; u: European Journal of Human Henetics. Supplement 13 (2005) (S1), 2005. str. 100-100 (poster, sažetak, znanstveni)
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43.Morožin-Pohovski, LeonaMikrodelecija 22q11 u fenotipski rizičnoj populaciji djece, 2004., magistarski rad, Prirodoslovno-matematički fakultet, Zagreb
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44.Barišić, Ingeborg; Petković, Iskra; Morožin Pohovski, Leona; Bagatin, Mario; Stipančić, GordanaMikrodelecija 22q11.2 u djece s rascjepom usne/nepca, hipokalcimijom i dismorfijom // Paediatria Croatica. Supplement, 48 (2004), suppl 2; 26-26 (podatak o recenziji nije dostupan, članak, znanstveni)
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45.Barišić, Ingeborg; Petković, Iskra; Morožin, LeonaClinical and cytogenetic findings in a patient with partial 8p duplication // Annales de Genetique, 46 (2003), Suppl 2-3. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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46.Petković, Iskra; Barišić, Ingeborg; Morožin, LeonaA new case of partial trisomy 16q // Book of Abstracts of the European Human Genetics Conference ; u: European Journal of Human Genetics. Supplement
Birmingham, Ujedinjeno Kraljevstvo, 2003. str. 124-124 (poster, međunarodna recenzija, sažetak, znanstveni) -
47.Barišić, Ingeborg; Petković, Iskra; Morožin, Leona, Devriendt, KoenInterstitial deletion of the short arm of chromosome 8 in a boy with mild phenotype and normal development // Abstracts of the ..... ; u: Annales de Genetique. Supplement ......, 2001. str. s69-s69 (poster, sažetak, znanstveni)
