pubmed-article:17179725 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C0020792 | lld:lifeskim |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C0271623 | lld:lifeskim |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C1415171 | lld:lifeskim |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C1522508 | lld:lifeskim |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C1513380 | lld:lifeskim |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
pubmed-article:17179725 | lifeskim:mentions | umls-concept:C0549217 | lld:lifeskim |
pubmed-article:17179725 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:17179725 | pubmed:dateCreated | 2007-3-9 | lld:pubmed |
pubmed-article:17179725 | pubmed:abstractText | Currently known mutations account for less than 15% of cases with normosmic hypogonadotropic hypogonadism (nIHH). The objective of the study was to identify novel hereditary associations in the pathogenesis of nIHH. | lld:pubmed |
pubmed-article:17179725 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17179725 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17179725 | pubmed:language | eng | lld:pubmed |
pubmed-article:17179725 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17179725 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:17179725 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17179725 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17179725 | pubmed:issn | 0028-3835 | lld:pubmed |
pubmed-article:17179725 | pubmed:author | pubmed-author:O'RahillyStep... | lld:pubmed |
pubmed-article:17179725 | pubmed:author | pubmed-author:MillarRobert... | lld:pubmed |
pubmed-article:17179725 | pubmed:author | pubmed-author:LuZhi-LiangZL | lld:pubmed |
pubmed-article:17179725 | pubmed:author | pubmed-author:FarooqiI... | lld:pubmed |
pubmed-article:17179725 | pubmed:author | pubmed-author:YukselBilginB | lld:pubmed |
pubmed-article:17179725 | pubmed:author | pubmed-author:TopalogluA... | lld:pubmed |
pubmed-article:17179725 | pubmed:author | pubmed-author:MunganNesliha... | lld:pubmed |
pubmed-article:17179725 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:17179725 | pubmed:volume | 84 | lld:pubmed |
pubmed-article:17179725 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17179725 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17179725 | pubmed:pagination | 301-8 | lld:pubmed |
pubmed-article:17179725 | pubmed:dateRevised | 2010-9-20 | lld:pubmed |
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pubmed-article:17179725 | pubmed:meshHeading | pubmed-meshheading:17179725... | lld:pubmed |
pubmed-article:17179725 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:17179725 | pubmed:articleTitle | Molecular genetic analysis of normosmic hypogonadotropic hypogonadism in a Turkish population: identification and detailed functional characterization of a novel mutation in the gonadotropin-releasing hormone receptor gene. | lld:pubmed |
pubmed-article:17179725 | pubmed:affiliation | Division of Paediatric Endocrinology and Metabolism, Cukurova University, Faculty of Medicine, Adana, Turkey. ktopaloglu@cu.edu.tr | lld:pubmed |
pubmed-article:17179725 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17179725 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
entrez-gene:2798 | entrezgene:pubmed | pubmed-article:17179725 | lld:entrezgene |
http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:17179725 | lld:entrezgene |