pubmed-article:12097805 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12097805 | lifeskim:mentions | umls-concept:C1263846 | lld:lifeskim |
pubmed-article:12097805 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
pubmed-article:12097805 | lifeskim:mentions | umls-concept:C0170657 | lld:lifeskim |
pubmed-article:12097805 | lifeskim:mentions | umls-concept:C0237753 | lld:lifeskim |
pubmed-article:12097805 | lifeskim:mentions | umls-concept:C0039290 | lld:lifeskim |
pubmed-article:12097805 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
pubmed-article:12097805 | lifeskim:mentions | umls-concept:C0237881 | lld:lifeskim |
pubmed-article:12097805 | lifeskim:mentions | umls-concept:C0750502 | lld:lifeskim |
pubmed-article:12097805 | lifeskim:mentions | umls-concept:C0439828 | lld:lifeskim |
pubmed-article:12097805 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:12097805 | pubmed:dateCreated | 2002-7-4 | lld:pubmed |
pubmed-article:12097805 | pubmed:abstractText | The purpose of this study was to evaluate the relationship between attention deficit hyperactivity disorder (ADHD) and polymorphism of the two regions of the 5-HTT gene [variable number of tandem repeats (VNTR) and 5-HTTLRR] in a sample of Turkish children. Using the PCR technique, these polymorphisms were assessed in 71 patients with ADHD and 128 healthy controls. The 5-HTTLPR S/S genotype was significantly lower in the patients than in the controls (p = 0.018). Homozygous and heterozygous L variant predominated in the ADHD group. But the VNTR STin2.12/12 genotype was significantly less found in the patients than in the controls (p = 0.001). There was no significant difference between the frequency of the short (S), long, 10, and 12 alleles of both groups. The lack of an S/S variant of 5-HTTLPR polymorphism of the STin2.12/12 variant of VNTR polymorphism appears to be associated with an increased risk of ADHD. | lld:pubmed |
pubmed-article:12097805 | pubmed:language | eng | lld:pubmed |
pubmed-article:12097805 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12097805 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:12097805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12097805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12097805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12097805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:12097805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12097805 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12097805 | pubmed:issn | 0302-282X | lld:pubmed |
pubmed-article:12097805 | pubmed:author | pubmed-author:Sava?Haluk... | lld:pubmed |
pubmed-article:12097805 | pubmed:author | pubmed-author:HerkenHasanH | lld:pubmed |
pubmed-article:12097805 | pubmed:author | pubmed-author:TutkunHamdiH | lld:pubmed |
pubmed-article:12097805 | pubmed:author | pubmed-author:Zoro?luSalih... | lld:pubmed |
pubmed-article:12097805 | pubmed:author | pubmed-author:ErdalMehmet... | lld:pubmed |
pubmed-article:12097805 | pubmed:author | pubmed-author:Ala?ehirliBel... | lld:pubmed |
pubmed-article:12097805 | pubmed:author | pubmed-author:ErdalNurtenN | lld:pubmed |
pubmed-article:12097805 | pubmed:author | pubmed-author:SivasliErcanE | lld:pubmed |
pubmed-article:12097805 | pubmed:copyrightInfo | Copyright 2002 S. Karger AG, Basel | lld:pubmed |
pubmed-article:12097805 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:12097805 | pubmed:volume | 45 | lld:pubmed |
pubmed-article:12097805 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12097805 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12097805 | pubmed:pagination | 176-81 | lld:pubmed |
pubmed-article:12097805 | pubmed:dateRevised | 2005-11-17 | lld:pubmed |
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pubmed-article:12097805 | pubmed:meshHeading | pubmed-meshheading:12097805... | lld:pubmed |
pubmed-article:12097805 | pubmed:year | 2002 | lld:pubmed |
pubmed-article:12097805 | pubmed:articleTitle | Significance of serotonin transporter gene 5-HTTLPR and variable number of tandem repeat polymorphism in attention deficit hyperactivity disorder. | lld:pubmed |
pubmed-article:12097805 | pubmed:affiliation | Department of Child and Adolescent Psychiatry, Faculty of Medicine, Gaziantep University, Kolejtepe, Gaziantep, Turkey. zoroglus@hotmail.com | lld:pubmed |
pubmed-article:12097805 | pubmed:publicationType | Journal Article | lld:pubmed |
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