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Prikaz rezultata 1-10 od 11
Screening for CFTR gene mutations and polymorphisms in patients with chronic pancreatitis
(Springernature, London, 2002)
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)
Functional analyses of the FIIc.*64_*66del gene variant and its potential role in fetal loss etiology
(Nature Publishing Group, London, 2018)
Detection rate of 22q11.2 microdeletion using strict diagnostic criteria
(Springer Nature, 2023)
Background/Objectives: 22q11.2 microdeletion, detected in
patients with 22q11.2 Deletion Syndrome (22q11.2DS), is the most
common microdeletion syndrome in humans. 22q11.2DS has high
risk for neurodevelopmental disorders ...
Metastatic colorectal cancer chemotherapeutic drugs alter the expression of TGF beta signaling-related miR-175p, miR-21-5p and miR-93-5p in vitro
(Nature Publishing Group, London, 2019)
22q11.2 microdeletion is the most common genomic abnormality in Serbian newborns with critical congenital heart disease and could be rapidly detected by Multiplex ligation probe amplification analysis
(Springer Nature, 2023)
Background/Objectives: Genetic tests may facilitate rapid and
effective diagnostics but unfortunately their high costs usually
limit their application in all patients (1). We aimed to investigate
the utility of rapid, ...
SOX3 function in glioblastoma cells
(Springernature, London, 2022)