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Sanja Cirkovic

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International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|October 23, 2013
Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from SerbiaMarijana Miskovic, Tanja Lalic, Danijela Radivojevic, et al.
The Tohoku Journal of Experimental Medicine|October 6, 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 SerbiaMarijana Miskovic, Tanja Lalic, Danijela Radivojevic, et al.
Journal of Pediatric Hematology/Oncology|January 7, 2009
Successful treatment of hodgkin lymphoma in nijmegen breakage syndromeAnkica Jovanovic, Predrag Minic, Marija Scekic-Guc, et al.
Journal of Pediatric Hematology/Oncology|December 31, 2024
Neuroblastoma Occurring in Nijmegen Breakage SyndromeMarina Djurisic, Adrijan Sarajlija, Danijela Radivojevic, et al.
BMC Medical Genetics|November 23, 2017
Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literatureCinthia Aguilera, Marina Viñas-Jornet, Neus Baena, et al.
Diseases (Basel, Switzerland)|June 25, 2026
From Suspected Congenital Cytomegalovirus Infection to Malan Syndrome: Delayed Genetic Diagnosis Due to Diagnostic AnchoringGordana Kovacevic, Sanja Cirkovic, Gordana Petrovic, et al.
Genes|June 27, 2024
Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity?Nikola Ilic, Nina Maric, Ales Maver, et al.
Molecular Cytogenetics|November 1, 2013
Complex small supernumerary marker chromosomes - an updateThomas Liehr, Sanja Cirkovic, Tanja Lalic, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|October 23, 2013
Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from SerbiaMarijana Miskovic, Tanja Lalic, Danijela Radivojevic, et al.
The Tohoku Journal of Experimental Medicine|October 6, 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 SerbiaMarijana Miskovic, Tanja Lalic, Danijela Radivojevic, et al.
Journal of Pediatric Hematology/Oncology|January 7, 2009
Successful treatment of hodgkin lymphoma in nijmegen breakage syndromeAnkica Jovanovic, Predrag Minic, Marija Scekic-Guc, et al.
Journal of Pediatric Hematology/Oncology|December 31, 2024
Neuroblastoma Occurring in Nijmegen Breakage SyndromeMarina Djurisic, Adrijan Sarajlija, Danijela Radivojevic, et al.
BMC Medical Genetics|November 23, 2017
Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literatureCinthia Aguilera, Marina Viñas-Jornet, Neus Baena, et al.
Diseases (Basel, Switzerland)|June 25, 2026
From Suspected Congenital Cytomegalovirus Infection to Malan Syndrome: Delayed Genetic Diagnosis Due to Diagnostic AnchoringGordana Kovacevic, Sanja Cirkovic, Gordana Petrovic, et al.
Genes|June 27, 2024
Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity?Nikola Ilic, Nina Maric, Ales Maver, et al.
Molecular Cytogenetics|November 1, 2013
Complex small supernumerary marker chromosomes - an updateThomas Liehr, Sanja Cirkovic, Tanja Lalic, et al.
Pageof 1