Read more about the article Seroprevalence and genotyping of hepatitis B, hepatitis C and HIV among healthy population and Turkish soldiers in Northern Cyprus.
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Seroprevalence and genotyping of hepatitis B, hepatitis C and HIV among healthy population and Turkish soldiers in Northern Cyprus.

Abstract To compare the prevalence of hepatitis viral markers among soldiers from Turkey, blood donors from Northern Cyprus, and soldiers from Northern Cyprus. Hepatitis B surface antigen (HBsAg), anti-HCV and…

Continue ReadingSeroprevalence and genotyping of hepatitis B, hepatitis C and HIV among healthy population and Turkish soldiers in Northern Cyprus.
Read more about the article A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease.
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A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease.

Abstract Charcot-Marie-Tooth (CMT) disease is the most common form of inherited motor and sensory neuropathy. Based on neurophysiological and neuropathological criteria CMT has been sub-classified into two main types: demyelinating…

Continue ReadingA novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease.
Read more about the article Delta-thalassemia in Cyprus.
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Delta-thalassemia in Cyprus.

Abstract To help clarify the hematological picture of patients who may be positive for beta- and delta-globin gene mutations, the following study was carried out. Our aim was to identify…

Continue ReadingDelta-thalassemia in Cyprus.
Read more about the article Vertigo and imbalance caused by a small lesion in the anterior insula.
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Vertigo and imbalance caused by a small lesion in the anterior insula.

Abstract The exact location of the vestibular cortex in humans has not yet been established. Isolated lesions in the insula are exceptional. We describe a patient with recurrent episodes of…

Continue ReadingVertigo and imbalance caused by a small lesion in the anterior insula.
Read more about the article Molecular homogeneity in diverse geographical populations of Phlebotomus papatasi (Diptera, Psychodidae) inferred from ND4 mtDNA and ITS2 rDNA Epidemiological consequences.
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Molecular homogeneity in diverse geographical populations of Phlebotomus papatasi (Diptera, Psychodidae) inferred from ND4 mtDNA and ITS2 rDNA Epidemiological consequences.

Abstract An intraspecific study on Phlebotomus papatasi, the main proven vector of Leishmania major among the members of the subgenus Phlebotomus, was performed. The internal transcribed spacer 2 (ITS 2)…

Continue ReadingMolecular homogeneity in diverse geographical populations of Phlebotomus papatasi (Diptera, Psychodidae) inferred from ND4 mtDNA and ITS2 rDNA Epidemiological consequences.
Read more about the article Genetic polymorphisms in the DNA repair genes XRCC1, XRCC2 and XRCC3 and risk of breast cancer in Cyprus.
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Genetic polymorphisms in the DNA repair genes XRCC1, XRCC2 and XRCC3 and risk of breast cancer in Cyprus.

Abstract Population-based studies have reported significant associations between specific genetic polymorphisms and breast cancer susceptibility. A number of studies have demonstrated that common variants of genes involved in the DNA…

Continue ReadingGenetic polymorphisms in the DNA repair genes XRCC1, XRCC2 and XRCC3 and risk of breast cancer in Cyprus.
Read more about the article Recombinant Sabin environmental isolates in Greece and Cyprus.
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Recombinant Sabin environmental isolates in Greece and Cyprus.

Abstract Twenty-one polioviruses (PVs) Sabin strains were isolated from sewage treatment plants from Metamorphosis, Athens, Greece during the time period from May to October 1996, and from two other sites…

Continue ReadingRecombinant Sabin environmental isolates in Greece and Cyprus.
Read more about the article Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.
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Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.

Abstract We studied 325 thalassemia intermedia patients from Iran, India, Pakistan, Thailand, Mauritius and Cyprus to examine factors which influence the phenotype. The beta-thalassemia (thal) mutations were determined for 219…

Continue ReadingMulticenter study of the molecular basis of thalassemia intermedia in different ethnic populations.
Read more about the article Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.
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Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.

Abstract The rapid advancement of high-resolution DNA copy number assessment methods revealed the significant contribution of submicroscopic genetic imbalances to abnormal phenotypes, including mental retardation. In order to detect submicroscopic…

Continue ReadingScreening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.