Danijela Radivojevic
Doctor of Philosophy - PhD, Faculty of Biology, University of Belgrade, Department of Genetics
- Serbian Genetic Society, Section of Medical Genetics
- European Society of Human Genetic (National Society's representative)
- Associate in international projects CFTR2
- European Molecular Genetics Quality Network assessor
- CF Genetic Analysis Consortium for cystic fibrosis
- European association for Cystic Fibrosis (CF Network)
- EuroGene test network, Orphanet
- Member of the editorial board of the international journal "Journal of Clinical Pediatrics and Neonatology"
Position: Head of Section of Molecular Genetics, Laboratory of Medical Genetics, Mother and Child Health Institute of Serbia
Jobs, responsibilities, interests:
- prenatal and postnatal diagnosis of chromosomal abnormalities, chromosomal diseases
- prenatal and postnatal diagnosis of Microdeletion Syndromes, cystic fibrosis, Duchenne and Becker muscular dystrophy, spinal muscular atrophy, hemophilia A, FraX Sy, AR-Non Syndromic Hearing Loss and Deafness
- changes in the genetic diseases and chromosomal instability-Nijmegen syndrome, Fancony anemia
- molecular and cytogenetic analysis of sex chromosomes, genetic causes of thrombophilia, sterility, infertility and spontaneous miscarriages
- genetic counseling
- accreditation, quality control for diagnostic medical laboratories
Supervisors: Supervisor
- Serbian Genetic Society, Section of Medical Genetics
- European Society of Human Genetic (National Society's representative)
- Associate in international projects CFTR2
- European Molecular Genetics Quality Network assessor
- CF Genetic Analysis Consortium for cystic fibrosis
- European association for Cystic Fibrosis (CF Network)
- EuroGene test network, Orphanet
- Member of the editorial board of the international journal "Journal of Clinical Pediatrics and Neonatology"
Position: Head of Section of Molecular Genetics, Laboratory of Medical Genetics, Mother and Child Health Institute of Serbia
Jobs, responsibilities, interests:
- prenatal and postnatal diagnosis of chromosomal abnormalities, chromosomal diseases
- prenatal and postnatal diagnosis of Microdeletion Syndromes, cystic fibrosis, Duchenne and Becker muscular dystrophy, spinal muscular atrophy, hemophilia A, FraX Sy, AR-Non Syndromic Hearing Loss and Deafness
- changes in the genetic diseases and chromosomal instability-Nijmegen syndrome, Fancony anemia
- molecular and cytogenetic analysis of sex chromosomes, genetic causes of thrombophilia, sterility, infertility and spontaneous miscarriages
- genetic counseling
- accreditation, quality control for diagnostic medical laboratories
Supervisors: Supervisor
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