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Browsing by Author Guc-Scekic, Marija P
Showing results 1 to 13 of 13
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2009 | A complex rearrangement involving cryptic deletion of ETV6 and CDKN1B genes in a case of childhood acute lymphoblastic leukemia | Krstic, Aleksandra Drago; Impera, Luciana; Guc-Scekic, Marija P; Lakic, Nina; Djokic, Dragan; Slavkovic, Bojana; Storlazzi, Clelia Tiziana | Article | 22M22 |
| 2008 | Analysis of extra- and intragenic marker haplotypes as part of molecular diagnosis of cystic fibrosis in patients from Serbia | Radivojevic, Danijela; Lalic, Tanja; Djurisic, Marina; Guc-Scekic, Marija P; Minic, Predrag B; Sovtic, Aleksandar D | Научни чланак | Мп категорија ће бити приказана накнадно. |
| 2013 | Complex small supernumerary marker chromosomes - an update | Liehr, Thomas; Cirkovic, Sanja S; Lalic, Tanja; Guc-Scekic, Marija P; ...; (broj, koautora 17) | Научни чланак | 22M22 - Међународни часопис категорије M22 |
| 2002 | Cytogenetic and molecular genetic characterization of patients with neuroblastoma in Yugoslavia | Djurisic, Marina; Guc-Scekic, Marija P; Radivojevic, Danijela; Lalic, Tanja; Djuricic, Slavisa M; Djokic, Dragan | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2005 | Deletion and duplication screening in the DMD gene using MLPA | Lalic, Tanja; Vossen, RH; Coffa, J; Schouten, JP; Guc-Scekic, Marija P; Radivojevic, Danijela; Djurisic, Marina; Breuning, MH; White, SJ; den, Dunnen JT | Article | 21M21 |
| 2002 | Genotype-phenotype correlations in a group of Yugoslavian adult cystic fibrosis patients | Radivojevic, Danijela; Djurisic, Marina; Minic, Predrag B; Guc-Scekic, Marija P; Lalic, Tanja | Conference Paper | Mp. category will be shown later |
| 2011 | Lower Incidence of Deletions in the Survival of Motor Neuron Gene and the Neuronal Apoptosis Inhibitory Protein Gene in Children with Spinal Muscular Atrophy from Serbia | Miskovic, Marijana; Lalic, Tanja; Radivojevic, Danijela; Cirkovic, Sanja S; Vlahovic, Gordana; Zamurovic, Dragan R; Guc-Scekic, Marija P | Article | 22M22 |
| 2000 | Minimally differentiated acute myeloid leukemia (AML-M0) in children: A single center experience | Kuzmanovic, Milos B; Rasovic, Nada; Bunjevacki, Gordana; Guc-Scekic, Marija P; Bunjevacki, Vera I | Article | 21aM21a |
| 2011 | Molecular characterization of a complex karyotype revealed cryptic deletion of the ETV6 and CDKN1B genes on 12p in the case of childhood B-ALL | Krstic, Aleksandra Drago; Impera, Luciana; Guc-Scekic, Marija P; Lakic, Nina; Djokic, Dragan; Slavkovic, Bojana; Storlazzi, Clelia Tiziana | Conference Paper | Mp. category will be shown later |
| 2003 | Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation | Major, Tamara | Article | 22M22 |
| 2004 | Spectrum of cystic fibrosis mutations in Serbia and Montenegro and strategy for prenatal diagnosis | Radivojevic, Danijela; Djurisic, Marina; Lalic, Tanja; Guc-Scekic, Marija P; Savic, Jovan; Minic, Predrag B; Antoniadi, T; Tzetis, M; Kanavakis, E | Article | 22M22 |
| 2014 | Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from Serbia | Miskovic, Marijana; Lalic, Tanja; Radivojevic, Danijela; Cirkovic, Sanja S; Ostojic, Slavica; Guc-Scekic, Marija P | Article | 22M22 |
| 2005 | Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21 | Riegel, M; Hargreaves, P; Baumer, A; Guc-Scekic, Marija P; Ignjatovic, M; Schinzel, A | Article | 23M23 |