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Genetic polymorphisms of FSHR, CYP17, CYP1A1, CAPN10, INSR, SERPINE1 genes in adolescent girls with polycystic ovary syndrome
BackgroundPolycystic ovary syndrome (PCOS), whose genetic basis is not completely well understood, is the most common endocrine disorder in women and it typically develops during adolescence. The aimExpand
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Significance of Serotonin Transporter Gene Polymorphism in Tinnitus
Objectives: To assess the role of serotonin transporter gene (SLC6A4) polymorphism in tinnitus. Materials and Methods: Fifty-four consecutive patients experiencing subjective tinnitus and 174 healthyExpand
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Serotonin transporter gene polymorphisms and sertraline response in major depression patients.
Major depression (MD) has a complex multifactorial etiology with genetic and environmental factors contributing to the disorder. As with all antidepressant treatments, there is variability in drugExpand
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PON1 55 and 192 Gene Polymorphisms in Type 2 Diabetes Mellitus Patients in a Turkish Population
Diabetes mellitus is a multifactorial metabolic disease, caused by the complete or relative absence of insulin hormone, which results in the deterioration of carbohydrate, protein, and lipidExpand
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GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals
This study aimed to assess mutations in GJB2 gene (connexin 26), as well as A1555G mitochondrial mutation in both the patients with profound genetic nonsyndromic hearing loss and healthy controls.Expand
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Association of GJB2 gene mutation with cochlear implant performance in genetic non-syndromic hearing loss.
OBJECTIVE To analyze the association of GJB2 gene mutations with cochlear implant performance in children. METHODS Sixty-five consecutive children who underwent cochlear implantation due toExpand
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Two Novel Missense Mutations in the Connexin 26 Gene in Turkish Patients with Nonsyndromic Hearing Loss
Most nonsyndromic hearing losses are caused by mutations in the GJB2 gene, and studies have revealed that the forms and frequencies of these mutations are largely dependent on ethnic origin. In theExpand
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Numerical chromosomal abnormalities detected by atomic force microscopy.
The numerical abnormalities of human metaphase chromosomes, fixed according to standard procedures for optical microscopy but not treated for banding, were detected by atomic force microscopy (AFM).Expand
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Determination of a translocation chromosome by atomic force microscopy.
Atomic force microscopy (AFM) has been used to study the translocation involving chromosomes 11 and 13. An amniocentesis procedure was performed at 18 weeks of pregnancy on a familial balancedExpand
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The mechanism of G-banding detected by atomic force microscopy.
The morphologic changes occurring in human chromosomes during G-banding by trypsin treatment on the same metaphase were followed with the aid of an atomic force microscope (AFM). It was found thatExpand
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