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Polymorphisms of vascular cell adhesion molecule1 (VCAM1) in polycystic ovary syndrome determined by quantitative real-time polymerase chain reaction and melting curve analysis
Abstract Objective Polycystic ovary syndrome (PCOS) is a common endocrinopathy associated with increased risk of obesity, insulin resistance (IR) and type 2 diabetes mellitus. Low-grade chronic inflammation and imbalance between pro- and anti-inflammatory cytokines has been proposed to play a role i...
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Published in: | European journal of obstetrics & gynecology and reproductive biology 2012-02, Vol.160 (2), p.174-178 |
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description | Abstract Objective Polycystic ovary syndrome (PCOS) is a common endocrinopathy associated with increased risk of obesity, insulin resistance (IR) and type 2 diabetes mellitus. Low-grade chronic inflammation and imbalance between pro- and anti-inflammatory cytokines has been proposed to play a role in the pathogenesis. Vascular cell adhesion molecule1 (VCAM1) is among the parameters reflecting low-grade chronic inflammation whose expression is increased by pro-inflammatory cytokines. This study examined the possible association of T-1591C and T-833C single nucleotide polymorphisms (SNPs) of VCAM1 gene with the occurrence and the clinical/biochemical characteristics of PCOS. Study design We analyzed genotype and allele distributions of the above-mentioned SNPs in DNA from peripheral blood leukocytes of 169 patients with PCOS and 179 healthy women, by a real-time polymerase chain reaction (PCR) method combined with melting curve analysis using fluorescence-labeled hybridization probes. Results No significant associations between PCOS and the variant alleles of VCAM1-1591 (OR: 1.09, 95% CI = 0.74–1.58) and -833 (OR: 1.42, 95% CI = 0.59–3.43) were observed. None of the studied polymorphisms was found to affect IR indices and sVCAM levels significantly. However, PCOS women heterozygous for VCAM1-1591 polymorphism (CT) had significant increased triglyceride and decreased HDL-C in comparison with wild homozygous (TT) ones. Conclusions Although there is no association between -1591 and -833 polymorphisms of VCAM1 gene and susceptibility to PCOS, higher triglyceride and lower HDL-C in VCAM1-1591 CT genotype suspect that heterozygous patients are prone to increased risk for atherosclerosis and cardiovascular disease. In addition, bearing in mind that PCOS is a consequence of interaction between various genetic and environmental factors, the association between heterozygocity of VCAM1-1591 polymorphism and some lipid parameters may depend on the impact of other known or unknown polymorphisms, being in linkage disequilibrium with this locus of VCAM1 gene. |
doi_str_mv | 10.1016/j.ejogrb.2011.11.013 |
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Low-grade chronic inflammation and imbalance between pro- and anti-inflammatory cytokines has been proposed to play a role in the pathogenesis. Vascular cell adhesion molecule1 (VCAM1) is among the parameters reflecting low-grade chronic inflammation whose expression is increased by pro-inflammatory cytokines. This study examined the possible association of T-1591C and T-833C single nucleotide polymorphisms (SNPs) of VCAM1 gene with the occurrence and the clinical/biochemical characteristics of PCOS. Study design We analyzed genotype and allele distributions of the above-mentioned SNPs in DNA from peripheral blood leukocytes of 169 patients with PCOS and 179 healthy women, by a real-time polymerase chain reaction (PCR) method combined with melting curve analysis using fluorescence-labeled hybridization probes. Results No significant associations between PCOS and the variant alleles of VCAM1-1591 (OR: 1.09, 95% CI = 0.74–1.58) and -833 (OR: 1.42, 95% CI = 0.59–3.43) were observed. None of the studied polymorphisms was found to affect IR indices and sVCAM levels significantly. However, PCOS women heterozygous for VCAM1-1591 polymorphism (CT) had significant increased triglyceride and decreased HDL-C in comparison with wild homozygous (TT) ones. Conclusions Although there is no association between -1591 and -833 polymorphisms of VCAM1 gene and susceptibility to PCOS, higher triglyceride and lower HDL-C in VCAM1-1591 CT genotype suspect that heterozygous patients are prone to increased risk for atherosclerosis and cardiovascular disease. In addition, bearing in mind that PCOS is a consequence of interaction between various genetic and environmental factors, the association between heterozygocity of VCAM1-1591 polymorphism and some lipid parameters may depend on the impact of other known or unknown polymorphisms, being in linkage disequilibrium with this locus of VCAM1 gene.</description><identifier>ISSN: 0301-2115</identifier><identifier>EISSN: 1872-7654</identifier><identifier>DOI: 10.1016/j.ejogrb.2011.11.013</identifier><identifier>PMID: 22137570</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Adolescent ; Adult ; Alleles ; Amino Acid Substitution ; Child ; Cholesterol, HDL - blood ; Female ; Gene Frequency ; Genetic Association Studies ; Heterozygote ; Hot Temperature ; Humans ; Hypertriglyceridemia - genetics ; Insulin Resistance ; Linkage Disequilibrium ; Nucleic Acid Denaturation ; Obstetrics and Gynecology ; Polycystic ovary syndrome ; Polycystic Ovary Syndrome - blood ; Polycystic Ovary Syndrome - genetics ; Polycystic Ovary Syndrome - metabolism ; Polycystic Ovary Syndrome - physiopathology ; Polymorphism ; Polymorphism, Single Nucleotide ; Promoter Regions, Genetic ; Turkey ; Vascular Cell Adhesion Molecule-1 - chemistry ; Vascular Cell Adhesion Molecule-1 - genetics ; Vascular cell adhesion molecule1 ; Young Adult</subject><ispartof>European journal of obstetrics & gynecology and reproductive biology, 2012-02, Vol.160 (2), p.174-178</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2011 Elsevier Ireland Ltd</rights><rights>Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-64eb719459102fc2b99462407e755b819e2e8c52804f679003bd9cab24eaacbc3</citedby><cites>FETCH-LOGICAL-c416t-64eb719459102fc2b99462407e755b819e2e8c52804f679003bd9cab24eaacbc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22137570$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kanmaz-Özer, Müge</creatorcontrib><creatorcontrib>Vural, Pervin</creatorcontrib><creatorcontrib>Doğru-Abbasoğlu, Semra</creatorcontrib><creatorcontrib>Gedikbaşı, Ali</creatorcontrib><creatorcontrib>Çil, Esra</creatorcontrib><creatorcontrib>Karadağ, Berrin</creatorcontrib><creatorcontrib>Uysal, Müjdat</creatorcontrib><title>Polymorphisms of vascular cell adhesion molecule1 (VCAM1) in polycystic ovary syndrome determined by quantitative real-time polymerase chain reaction and melting curve analysis</title><title>European journal of obstetrics & gynecology and reproductive biology</title><addtitle>Eur J Obstet Gynecol Reprod Biol</addtitle><description>Abstract Objective Polycystic ovary syndrome (PCOS) is a common endocrinopathy associated with increased risk of obesity, insulin resistance (IR) and type 2 diabetes mellitus. Low-grade chronic inflammation and imbalance between pro- and anti-inflammatory cytokines has been proposed to play a role in the pathogenesis. Vascular cell adhesion molecule1 (VCAM1) is among the parameters reflecting low-grade chronic inflammation whose expression is increased by pro-inflammatory cytokines. This study examined the possible association of T-1591C and T-833C single nucleotide polymorphisms (SNPs) of VCAM1 gene with the occurrence and the clinical/biochemical characteristics of PCOS. Study design We analyzed genotype and allele distributions of the above-mentioned SNPs in DNA from peripheral blood leukocytes of 169 patients with PCOS and 179 healthy women, by a real-time polymerase chain reaction (PCR) method combined with melting curve analysis using fluorescence-labeled hybridization probes. Results No significant associations between PCOS and the variant alleles of VCAM1-1591 (OR: 1.09, 95% CI = 0.74–1.58) and -833 (OR: 1.42, 95% CI = 0.59–3.43) were observed. None of the studied polymorphisms was found to affect IR indices and sVCAM levels significantly. However, PCOS women heterozygous for VCAM1-1591 polymorphism (CT) had significant increased triglyceride and decreased HDL-C in comparison with wild homozygous (TT) ones. Conclusions Although there is no association between -1591 and -833 polymorphisms of VCAM1 gene and susceptibility to PCOS, higher triglyceride and lower HDL-C in VCAM1-1591 CT genotype suspect that heterozygous patients are prone to increased risk for atherosclerosis and cardiovascular disease. In addition, bearing in mind that PCOS is a consequence of interaction between various genetic and environmental factors, the association between heterozygocity of VCAM1-1591 polymorphism and some lipid parameters may depend on the impact of other known or unknown polymorphisms, being in linkage disequilibrium with this locus of VCAM1 gene.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Alleles</subject><subject>Amino Acid Substitution</subject><subject>Child</subject><subject>Cholesterol, HDL - blood</subject><subject>Female</subject><subject>Gene Frequency</subject><subject>Genetic Association Studies</subject><subject>Heterozygote</subject><subject>Hot Temperature</subject><subject>Humans</subject><subject>Hypertriglyceridemia - genetics</subject><subject>Insulin Resistance</subject><subject>Linkage Disequilibrium</subject><subject>Nucleic Acid Denaturation</subject><subject>Obstetrics and Gynecology</subject><subject>Polycystic ovary syndrome</subject><subject>Polycystic Ovary Syndrome - blood</subject><subject>Polycystic Ovary Syndrome - genetics</subject><subject>Polycystic Ovary Syndrome - metabolism</subject><subject>Polycystic Ovary Syndrome - physiopathology</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Promoter Regions, Genetic</subject><subject>Turkey</subject><subject>Vascular Cell Adhesion Molecule-1 - chemistry</subject><subject>Vascular Cell Adhesion Molecule-1 - genetics</subject><subject>Vascular cell adhesion molecule1</subject><subject>Young Adult</subject><issn>0301-2115</issn><issn>1872-7654</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFUtuKFDEQbURxx9U_EMmb60OPqfRt8iIsgzdYUfDyGtLpmp2M6WQ2lR7ov_ITTTOrD74YCgKVc06Rc6oongNfA4f29WGNh3Ab-7XgAOtcHKoHxQo2nSi7tqkfFitecSgFQHNRPCE68HyqSj4uLoSAqms6vip-fQluHkM87i2NxMKOnTSZyenIDDrH9LBHssGzMTjMfQR29WN7_QleMevZMZPNTMkaFk46zoxmP8QwIhswYRytx4H1M7ubtE826WRPyCJqVyabQQt9xKgJmdnrrJefTFqmaT-wEV2y_paZKWaW9trNZOlp8WinHeGz-_uy-P7u7bfth_Lm8_uP2-ub0tTQprKtse9A1o0ELnZG9FLWrah5h13T9BuQKHBjGrHh9a7tZDamH6TRvahRa9Ob6rJ4edY9xnA3ISU1Wlos0R7DREqCFKIRrczI-ow0MRBF3KljtGN2QwFXS1TqoM5RqSUqlStHlWkv7gdM_YjDX9KfbDLgzRmA-Zsni1GRsegNDjaiSWoI9n8T_hUwznprtPuJM9IhTDGbSgoUCcXV12Vdlm0B4Lytqrb6DQDGv3w</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Kanmaz-Özer, Müge</creator><creator>Vural, Pervin</creator><creator>Doğru-Abbasoğlu, Semra</creator><creator>Gedikbaşı, Ali</creator><creator>Çil, Esra</creator><creator>Karadağ, Berrin</creator><creator>Uysal, Müjdat</creator><general>Elsevier Ireland Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120201</creationdate><title>Polymorphisms of vascular cell adhesion molecule1 (VCAM1) in polycystic ovary syndrome determined by quantitative real-time polymerase chain reaction and melting curve analysis</title><author>Kanmaz-Özer, Müge ; Vural, Pervin ; Doğru-Abbasoğlu, Semra ; Gedikbaşı, Ali ; Çil, Esra ; Karadağ, Berrin ; Uysal, Müjdat</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-64eb719459102fc2b99462407e755b819e2e8c52804f679003bd9cab24eaacbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Alleles</topic><topic>Amino Acid Substitution</topic><topic>Child</topic><topic>Cholesterol, HDL - blood</topic><topic>Female</topic><topic>Gene Frequency</topic><topic>Genetic Association Studies</topic><topic>Heterozygote</topic><topic>Hot Temperature</topic><topic>Humans</topic><topic>Hypertriglyceridemia - genetics</topic><topic>Insulin Resistance</topic><topic>Linkage Disequilibrium</topic><topic>Nucleic Acid Denaturation</topic><topic>Obstetrics and Gynecology</topic><topic>Polycystic ovary syndrome</topic><topic>Polycystic Ovary Syndrome - blood</topic><topic>Polycystic Ovary Syndrome - genetics</topic><topic>Polycystic Ovary Syndrome - metabolism</topic><topic>Polycystic Ovary Syndrome - physiopathology</topic><topic>Polymorphism</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Promoter Regions, Genetic</topic><topic>Turkey</topic><topic>Vascular Cell Adhesion Molecule-1 - chemistry</topic><topic>Vascular Cell Adhesion Molecule-1 - genetics</topic><topic>Vascular cell adhesion molecule1</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kanmaz-Özer, Müge</creatorcontrib><creatorcontrib>Vural, Pervin</creatorcontrib><creatorcontrib>Doğru-Abbasoğlu, Semra</creatorcontrib><creatorcontrib>Gedikbaşı, Ali</creatorcontrib><creatorcontrib>Çil, Esra</creatorcontrib><creatorcontrib>Karadağ, Berrin</creatorcontrib><creatorcontrib>Uysal, Müjdat</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of obstetrics & gynecology and reproductive biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kanmaz-Özer, Müge</au><au>Vural, Pervin</au><au>Doğru-Abbasoğlu, Semra</au><au>Gedikbaşı, Ali</au><au>Çil, Esra</au><au>Karadağ, Berrin</au><au>Uysal, Müjdat</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymorphisms of vascular cell adhesion molecule1 (VCAM1) in polycystic ovary syndrome determined by quantitative real-time polymerase chain reaction and melting curve analysis</atitle><jtitle>European journal of obstetrics & gynecology and reproductive biology</jtitle><addtitle>Eur J Obstet Gynecol Reprod Biol</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>160</volume><issue>2</issue><spage>174</spage><epage>178</epage><pages>174-178</pages><issn>0301-2115</issn><eissn>1872-7654</eissn><abstract>Abstract Objective Polycystic ovary syndrome (PCOS) is a common endocrinopathy associated with increased risk of obesity, insulin resistance (IR) and type 2 diabetes mellitus. Low-grade chronic inflammation and imbalance between pro- and anti-inflammatory cytokines has been proposed to play a role in the pathogenesis. Vascular cell adhesion molecule1 (VCAM1) is among the parameters reflecting low-grade chronic inflammation whose expression is increased by pro-inflammatory cytokines. This study examined the possible association of T-1591C and T-833C single nucleotide polymorphisms (SNPs) of VCAM1 gene with the occurrence and the clinical/biochemical characteristics of PCOS. Study design We analyzed genotype and allele distributions of the above-mentioned SNPs in DNA from peripheral blood leukocytes of 169 patients with PCOS and 179 healthy women, by a real-time polymerase chain reaction (PCR) method combined with melting curve analysis using fluorescence-labeled hybridization probes. Results No significant associations between PCOS and the variant alleles of VCAM1-1591 (OR: 1.09, 95% CI = 0.74–1.58) and -833 (OR: 1.42, 95% CI = 0.59–3.43) were observed. None of the studied polymorphisms was found to affect IR indices and sVCAM levels significantly. However, PCOS women heterozygous for VCAM1-1591 polymorphism (CT) had significant increased triglyceride and decreased HDL-C in comparison with wild homozygous (TT) ones. Conclusions Although there is no association between -1591 and -833 polymorphisms of VCAM1 gene and susceptibility to PCOS, higher triglyceride and lower HDL-C in VCAM1-1591 CT genotype suspect that heterozygous patients are prone to increased risk for atherosclerosis and cardiovascular disease. In addition, bearing in mind that PCOS is a consequence of interaction between various genetic and environmental factors, the association between heterozygocity of VCAM1-1591 polymorphism and some lipid parameters may depend on the impact of other known or unknown polymorphisms, being in linkage disequilibrium with this locus of VCAM1 gene.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>22137570</pmid><doi>10.1016/j.ejogrb.2011.11.013</doi><tpages>5</tpages></addata></record> |
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subjects | Adolescent Adult Alleles Amino Acid Substitution Child Cholesterol, HDL - blood Female Gene Frequency Genetic Association Studies Heterozygote Hot Temperature Humans Hypertriglyceridemia - genetics Insulin Resistance Linkage Disequilibrium Nucleic Acid Denaturation Obstetrics and Gynecology Polycystic ovary syndrome Polycystic Ovary Syndrome - blood Polycystic Ovary Syndrome - genetics Polycystic Ovary Syndrome - metabolism Polycystic Ovary Syndrome - physiopathology Polymorphism Polymorphism, Single Nucleotide Promoter Regions, Genetic Turkey Vascular Cell Adhesion Molecule-1 - chemistry Vascular Cell Adhesion Molecule-1 - genetics Vascular cell adhesion molecule1 Young Adult |
title | Polymorphisms of vascular cell adhesion molecule1 (VCAM1) in polycystic ovary syndrome determined by quantitative real-time polymerase chain reaction and melting curve analysis |
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