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Browsing by Author Guc-Scekic, Marija P

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