Pregled po projektu: 072777
Pronađeno 49 radova
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26.Barišić, Ingeborg; Clementi Maurizio, Gjergja-Matejić, Romana; Stoll, Claude and EUROSACAN Study GroupPrenatal ultrasound detection of abdominal wall defects: associated malformations, chromosomal abnormalities and perinatal outcome // 6th European Symposium on the Prevention of Congenital Anomalies / Ettore, Giuseppe; Bianca, Sebastiano (ur.).
Catania: TM, Mangano Venera, 2001. str. 105-106 (predavanje, međunarodna recenzija, sažetak, znanstveni) -
27.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)
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28.Knežević, Jasna; Milić, Ana; Barišić, Ingeborg; Pavelić, JasminkaEvidence for 621+1 G T mutation in Croatian Population // Abstracts of the ..... ; u: European Journal of Human Genetics 9 (2001) (1), 2001. str. 173-173 (poster, sažetak, znanstveni)
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29.Bago, Ružica; Hećimović, Silva; Barišić, Ingeborg; Čulić, Vida; Pavelić, KrešimirDifferent distribution of DXS548 and FRAXAC1 haplotypes between normal and fragile X population in Croatia // 2nd International Conference on Signal Transduction. European Journal of Human Genetics 9(1), 2001
Cavtat, Hrvatska; Dubrovnik, Hrvatska, 2001. str. 284-284 (poster, sažetak, znanstveni) -
30.Petković, Iskra; Barišić, IngeborgApplication of fluorescence in situ hybridization (FISH) in clinical genetics // Paediatria Croatica, 45 (2001), 4; 175-178 (međunarodna recenzija, članak, znanstveni)
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31.Gjergja, Romana; Barišić, Ingeborg; Hećimović, Silva; Tanacković, Goranka; Sertić, Jadranka; Knežević, Jasna; Milić, Ana; Pavelić, KrešimirGenotype-phenotype correlation in Croatian cystic fibrosis patients // 2nd International Conference on Signal Transduction. European Journal of Human Genetics 9(1), 2001
Cavtat, Hrvatska; Dubrovnik, Hrvatska, 2001. str. 205-205 (poster, sažetak, znanstveni) -
32.Barišić, Ingeborg; Peter, Branimir; Juretić, Emilija; Mikecin, LiliToriello-Carey syndrome:further delineation and report of three new cases // European Journal of Human Genetics, 9 (2001), 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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33.Petković, Iskra; Barišić, IngeborgUnusual mosaicism due to non-homologous postzygotic recombination involving chromosomes 6 and 10 in the mother, and 46,Xder(X)t(X;6) in her daughter // European Journal of Human Genetics, 9 (2001), 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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34.Barišić, Ingeborg; Clementi, Maurizio; Haeusler, Martin; Gjergja, Romana; Kern, Josipa; Stoll, ClaudeEvaluation of prenatal ultrasound diagnosis of fetal abdominal wall defects by 19 European registries // Ultrasound in Obstetrics and Gynecology, 18 (2001), 4; 309-316 (međunarodna recenzija, članak, znanstveni)
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35.Hećimović, Silva; Vlašić, Jelena; Barišić, Ingeborg; Marković, Dubravko; Čulić, Vida; Pavelić, KrešimirA simple and rapid analysis of triplet repeat diseases by Expand Long PCR // Clinical Chemistry and Laboratory Medicine, 39 (2001), 12; 1259-1262 (međunarodna recenzija, članak, znanstveni)
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36.Primorac, Dragan; Rowe, David, W; Mottes, Monica; Barišić, Ingeborg; Antičević, Darko; Mirandola, Stefania; Gomez Lira, Macarena; Kalajzić, Ivo; Kušec, Vesna; Glorieux, Francis, HOsteogenesis imperfecta at the beginning of bone and joint decade // Croatian Medical Journal, 42 (2001), 4; 393-415 (podatak o recenziji nije dostupan, pregledni rad, ostalo)
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37.Ligutić, Ivo; Barišić, Ingeborg; Antičević, Darko; Vrdoljak, Javor; Primorac, Dragan;Koštane displazije - specifična zdravstvena skrb djece s hondrodisplazijama // Paediatria Croatica, 45 (2001), 1; 19-26 (podatak o recenziji nije dostupan, pregledni rad, stručni)
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38.Barišić, Ingeborg; Haeusler, Martin; Clementi, Maurizio; Gjergja-Matejić, Romana; Stoll, ClaudePrenatal ultrasound detection of abdominal wall defects: associated malformations, chromosomal abnormalities and pregnancy outcome // European journal of human genetics, 1 (2000), 8. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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39.Petković, Iskra; Barišić, IngeborgChromosome inactivation pattern study in an unbalanced X;6 translocation // European journal of human genetics, 1 (2000), 8. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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40.Barišić, Ingeborg; Clementi, Maurizio; Haeusler, Martin; Gjergja-Matejić, RomanaEvaluation of routine prenatal ultrasound detection of fetal gastrointestinal malformations: European multicentric study // Ultrasound in obstetrics & gynecology, 16 (2000), 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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41.Barišić, Ingeborg; Clementi, Maurizio; Haeusler, Martin; Gjergja, Romana; Modrušan-Mozetič, Zlata; Žužek, Adele; Stanojević, Milan; Beer, Zlata; Stoll, Claude; EUROSCAN Study GroupEvaluacija prenatalnog otkrivanja dijafragmalnih hernija rutinskim ultrazvučnim pregledom u 19 europskih centara // Paediatria Croatica, 44 (2000), 3. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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42.Barišić, Ingeborg; Stoll, Claude; Clementi, Maurizio; Haeusler, Martin; Gjergja-Matejić, Romana; Modrušan-Mozetič, Zlata; Žužek, Adele; Stanojević, Milan; Beer, Zlata; EUROSCAN Study GroupUčinkovitost prenatalnog ultrazvučnog otkrivanja kongenitalnih malformacija: europsko multicentrično ispitivanje // Paediatria Croatica, 44 (2000), 3. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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43.Barišić, Ingeborg; Clementi, Maurizio; Haeusler, Martin; Gjergja, Romana; Modrušan-Mozetič, Zlata; Žužek, Adele, Stanojević, Milan; Beer, Zlata; Stoll, Claude; EUROSCAN Study GroupEvaluation of prenatal ultrasound detection of fetal abdominal wall defects: European multicentric study // Proceedings of the XXII Alpe Adria Meeting of Perinatal Medicine ( XIV Congress) / Dražančić, Ante; Elkaz, B. (ur.).
Čakovec: Zrinski, dd, 2000. (predavanje, međunarodna recenzija, sažetak, znanstveni) -
44.Tanacković G, Barišić I, Gjergja-Matejić R, Hećimović S, Pavelić J.Tanacković, Goranka; Barišić, Ingeborg; Gjergja-Matejić, Romana; Hećimović, Silva; Pavelić, Jasminka // Clinical Genetics, 58 (2000), 4; 333-5. (međunarodna recenzija, pismo, znanstveni)
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45.Barišić, Ingeborg; Petković, Iskra; Mrsić, Sanja; Gjergja-Matejić, RomanaCitogenetička i FISH analiza u dječaka sa sindromom 48, XXYY // Paediatria Croatica, 44 (2000), 1-2; 65-68 (podatak o recenziji nije dostupan, članak, stručni)
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46.Barišić, Ingeborg; Juretić, Emilija; Peter, Branimir; Mikecin, Lili; Gjergja-Matejić RomanaToriello-Carey syndrome in two siblings: further delineation and confirmation of an autosomal recessive inheritance // European Journal of Human Genetics, 7 (1999), 1-2. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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47.Tanacković, Goranka; Barišić, Ingeborg; Pavelić, KrešimirThe occurrence of the most common CFTR mutations among Croatian cystic fibrosis patients // European Journal of Human Genetics, 7 (1999), Suppl 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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48.Barišić, Ingeborg; Petković, Iskra; Morožin, LeonaDe novo interstitial deletion of 8p21-p23 in a patient with dysmorphic features and normal development // Cytogenetics and Cell Genetics, 85 (1999), 1-2. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
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49.Barišić, Ingeborg; Marušić-Della Marina, Branka; Hećimović, Silva; Lujić, Lucija; Gjergja-Matejić, RomanaEpilepsija i EEG zapisi u bolesnika s mutacijomm u FMR1 genu // Paediatria Croatica, 43 (1999), 3; 105-110 (međunarodna recenzija, članak, znanstveni)
