14 Artículos
Original Article
Acceso abierto | 29 oct 2018
Family history as an important factor for stratifying participants in genetic studies of major depression
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Acceso abierto | 29 oct 2018
Detecting EGFR mutations in patients with non-small cell lung cancer
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Acceso abierto | 29 oct 2018
Analysis of the PPARD gene expression level changes in football players in response to the training cycle
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Acceso abierto | 29 oct 2018
Association of E-selectin S128R polymorphism with hereditary breast carcinoma susceptibility in Turkish patients without BRCA1/2 germline mutations
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Acceso abierto | 29 oct 2018
ADRB2 gene polymorphisms and salbutamol responsiveness in Serbian children with asthma
, , , y
Acceso abierto | 29 oct 2018
PPAR𝛾 gene and atherosclerosis: Genetic polymorphisms, epigenetics and therapeutic implications
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Acceso abierto | 29 oct 2018
Clinical variability in two Macedonian families with Arterial tortuosity syndrome
, , , , , , y
Acceso abierto | 29 oct 2018
The mitochondrial tRNAGly T10003C mutation may not be associated with diabetes mellitus
, y
Acceso abierto | 29 oct 2018
UGT1A1 (TA)n promoter genotype: Diagnostic and population pharmacogenetic marker in Serbia
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Acceso abierto | 29 oct 2018
Mutation in Phospholipase C, δ1 (PLCD1 ) gene underlies hereditary leukonychia in a Pashtun family and review of the literature
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Letter to the Editor
Acceso abierto | 29 oct 2018
Problems of unknown significance: Counseling in the era of next generation sequencing
Case Report
Acceso abierto | 29 oct 2018
Hyperinsulinism-hyperammonemia syndrome in an infant with seizures
, , , y
Acceso abierto | 29 oct 2018
Floating-Harbor syndrome: Presentation of the first Romanian patient with a SRCAP mutation and review of the literature
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Acceso abierto | 29 oct 2018
Acute pre-B lymphoblastic leukemia and congenital anomalies in a child with a de novo 22q11.1q11.22 duplication
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