Pregled po CROSBI profilu: Leona Morožin Pohovski (CROSBI Profil: 22012, MBZ: 261772)
Pronađeno 47 radova
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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)
