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Application of Next-Generation Sequencing Technology and Establishment of Biobanks
(Karger, Basel, 2018)
Institute of Molecular Genetics and Genetic Engineering has
become widely recognized as an expert centre for rare diseases
(RD). It is the first institution is Serbia that applied NGS methodology in research and diagnostics ...
New transcriptional regulatory element within the intron of phenylalanine hydroxylase gene
(Academic Press Inc Elsevier Science, San Diego, 2009)
Can anticoagulant therapy improve the outcome of pregnancy in thrombophilic women?
(Pergamon-Elsevier Science Ltd, Oxford, 2011)
Functional analysis and phenotypic outcome of S231F mutation in phenylalanine hydroxylase gene
(Springer, Dordrecht, 2008)
Tumor necrosis factor, tumor necrosis factor receptors type 1 and 2, lymphotoxin-alpha gene polymorphism in lymphoproliferative diseases in Serbian population
(Wiley-Blackwell Publishing, Inc, Malden, 2009)
Monoclonal gammopathy and lymphocyte clonality in patients with gaucher disease
(Elsevier, Bridgewater, 2008)
Pregnancy loss and thrombotic complications during pregnancy and puerperium in women with coinheritance of factor V Leiden and FII G20210A mutation
(Pergamon-Elsevier Science Ltd, Oxford, 2005)
8 year experience in molecular prenatal diagnostics of cystic fibrosis in Yugoslavia - problems and future trends
(Springernature, London, 1998)
Mutation analysis of CFTR gene in men with azoospermia
(Springernature, London, 1998)
Capacity Building for Rare Genomics
(Karger, Basel, 2018)
Infrequent occurrence of rare diseases (RD) has led to prolonged time needed to make an accurate diagnosis. Research and
development of new treatments has been insufficient due to the
narrow market for affected patients. ...