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Associate Professor

Valeria Marton

Department of Clinical Medicine
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  • Isrie, Mala; Breuss, Martin; Tian, Guoling; Hansen, Andi Harley; Cristofoli, Francesca; Morandell, Jasmin; Kupchinsky, Zachari A.; Sifrim, Alejandro; Rodriguez-Rodriguez, Celia Maria; Dapena, Elena Porta; Doonanco, Kurston; Leonard, Norma; Tinsa, Faten; Moortgat, Stéphanie; Ulucan, Hakan; Koparir, Erkan; Karaca, Ender; Katsanis, Nicholas; Marton, Valeria; Vermeesch, Joris Robert; Davis, Erica E.; Cowan, Nicholas J.; Keays, David Anthony; Van Esch, Hilde. Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. American Journal of Human Genetics 2015; Volum 97 (6). ISSN 0002-9297.s 790 - 800.s doi: 10.1016/j.ajhg.2015.10.014.

  • Klingenberg, Claus; Marton, valeria; Nystad, Mona. ”Metodehåndbok på Barneavdelinga på UNN. Kapittel 1:Kromosomanalyser, kromosomfeil, genetikk” C. Klingenberg, V. Marton og M. Nystad. 2012.

  • Nystad, Mona; Jørgensen, Agnete; Nilssen, Øivind; Marton, valeria. Delineation of syndromic Wolff-Parkinson-White due to 20p12.3 microdeletion of BMP2 region in a boy, his sister and their mosaic mother. European Society of Human Genetics (ESHG) Conference 2012, Nurnberg, Germany 23.06-26.06.2012 2012.

  • Marton, Valeria. "Nå ska du høre ka æ mene med arv". 2006 (90) ISBN 82-90263-01-5.

  • Klingenberg, Claus; Marton, valeria; Nystad, Mona. ”Metodehåndbok på Barneavdelinga på UNN. Kapittel 1:Kromosomanalyser, kromosomfeil, genetikk” C. Klingenberg, V. Marton og M. Nystad. 2012.

  • Nystad, Mona; Jørgensen, Agnete; Nilssen, Øivind; Marton, valeria. Delineation of syndromic Wolff-Parkinson-White due to 20p12.3 microdeletion of BMP2 region in a boy, his sister and their mosaic mother. European Society of Human Genetics (ESHG) Conference 2012, Nurnberg, Germany 23.06-26.06.2012 2012.

  • Marton, Valeria. "Nå ska du høre ka æ mene med arv". 2006 (90) ISBN 82-90263-01-5.

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