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Pregled prema Autor Jelisavcic, Marko

Prikaz rezultata 1 do 5 od 5
GodinaNaslovAutor(i)Tip rezultataMp-kat.
2013A case of a patient with multiple sSMC without phenotypic effectVesic, Marija; Jelisavcic, Marko; Niksic, Snezana B; Cuturilo, Goran; Ivanovic-Deretic, Vesna; Liehr, ThomasKonferencijski rad
Mp kategorija će biti prikazana naknadno.
2011A case of familial paracentric inversion of the short arm of the X chromosome (p21.2p11.23) associated with mental retardationVesic, Marija; Jelisavcic, Marko; Niksic, Snezana B; Pilic, Gordana; Misojcic, Aleksandar MKonferencijski rad
Mp kategorija će biti prikazana naknadno.
2011Evaluation of structural chromosomal abnormalities in couples with recurrent miscarriages and prenatal amniocentesisNiksic, Snezana B; Pilic, Gordana; Vesic, Marija; Jelisavcic, Marko; Misojcic, Aleksandar MKonferencijski rad
Mp kategorija će biti prikazana naknadno.
2012Family Paracentric Inversion of the Short Arm of Chromosome X (Xp21.2p11.23) and Connection with Autism Spectrum DisordersPejović-Milovančević, Milica  ; Vesic, Marija; Jelisavcic, Marko; Niksic, Snezana; Radivojevic-Pilic, Gordana; Mandic-Maravic, VanjaNaučni članak
23M23 - Međunarodni časopis kategorije M23
2005First and second trimester prenatal screening for chromosomal abnormality: the results of four years study (2001-2004)Brankovic-Niksic, Snezana; Pilic, Gordana; Nikolic, Sanja; Jelisavcic, Marko; Savic, SKonferencijski rad
Mp kategorija će biti prikazana naknadno.