CrossRef Text and Data Mining
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Is catechol-o-methyltransferase gene polymorphism a risk factor in the development of premenstrual syndrome?
Esma Ozturk Deveci, Adnan Incebiyik, Salih Selek, Aysun Camuzcuoglu, Nese Gul Hilali, Hakan Camuzcuoglu, Mehmet Emin Erdal, Mehmet Vural
Clin Exp Reprod Med. 2014;41(2):62-67.   Published online June 30, 2014
DOI: https://doi.org/10.5653/cerm.2014.41.2.62

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Is catechol-o-methyltransferase gene polymorphism a risk factor in the development of premenstrual syndrome?
Clinical and Experimental Reproductive Medicine. 2014;41(2):62   Crossref logo
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Catechol-O-methyltransferase gene polymorphism in women with polycystic ovary syndrome
Fertility and Sterility. 2008;90:S484   Crossref logo
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Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome
Rheumatology International. 2003;23(3):104-107   Crossref logo
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Catechol-O-Methyltransferase (COMT) val158met Polymorphism as a Risk Factor for PTSD
Comprehensive Guide to Post-Traumatic Stress Disorders. 2016;1019-1031   Crossref logo
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Catechol-O-Methyltransferase (COMT) val158met Polymorphism as a Risk Factor for PTSD
Comprehensive Guide to Post-Traumatic Stress Disorder. 2015;1-11   Crossref logo
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Functional catechol-O-methyltransferase gene polymorphism and susceptibility to schizophrenia
European Neuropsychopharmacology. 2002;12(4):299-303   Crossref logo
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Association between Catechol-O-methyltransferase rs4680 (G > A) polymorphism and lung cancer risk
Diagnostic Pathology. 2014;9(1):   Crossref logo
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Catechol-O-methyltransferase Gene Polymorphism (Val158Met) and Development of Pre-eclampsia
Archives of Medical Research. 2017;48(2):180-186   Crossref logo
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The Val158Met polymorphism of the catechol-O-methyltransferase gene is not associated with the risk of sporadic or latent prostate cancer in Japanese men
International Journal of Urology. 2007;14(9):800-804   Crossref logo
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Association between the catechol-o-methyltransferase val158met polymorphism with susceptibility and severity of carpal tunnel syndrome
Balkan Journal of Medical Genetics. 2015;18(2):43-48   Crossref logo
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