| pubmed-article:6789676 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:6789676 | lifeskim:mentions | umls-concept:C0042333 | lld:lifeskim |
| pubmed-article:6789676 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
| pubmed-article:6789676 | lifeskim:mentions | umls-concept:C0087090 | lld:lifeskim |
| pubmed-article:6789676 | lifeskim:mentions | umls-concept:C0241764 | lld:lifeskim |
| pubmed-article:6789676 | lifeskim:mentions | umls-concept:C1420598 | lld:lifeskim |
| pubmed-article:6789676 | lifeskim:mentions | umls-concept:C0023688 | lld:lifeskim |
| pubmed-article:6789676 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
| pubmed-article:6789676 | lifeskim:mentions | umls-concept:C1514697 | lld:lifeskim |
| pubmed-article:6789676 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:6789676 | pubmed:dateCreated | 1981-9-25 | lld:pubmed |
| pubmed-article:6789676 | pubmed:abstractText | A genetically determined, polymorphic electrophoretic variant of thyroxin-binding alpha-globulin (TBG) is found in sera from populations of African and Oceania origin, although not in Caucasians nor Orientals. The TBG polymorphism is inherited in X-linked fashion, based on data from American blacks, and thus provides an X-chromosome marker with a relatively high gene frequency in this ethnic group (frequency of the slow allele, TBGs, is 11%). This slow variant should prove valuable in expanding the map of the X chromosome and in linkage studies. An additional family exhibiting X-linked TBG deficiency is also described. | lld:pubmed |
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| pubmed-article:6789676 | pubmed:language | eng | lld:pubmed |
| pubmed-article:6789676 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:6789676 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:6789676 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:6789676 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:6789676 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:6789676 | pubmed:issn | 0002-9297 | lld:pubmed |
| pubmed-article:6789676 | pubmed:author | pubmed-author:WangLL | lld:pubmed |
| pubmed-article:6789676 | pubmed:author | pubmed-author:Cavalli-Sforz... | lld:pubmed |
| pubmed-article:6789676 | pubmed:author | pubmed-author:DaigerS PSP | lld:pubmed |
| pubmed-article:6789676 | pubmed:author | pubmed-author:RummelD PDP | lld:pubmed |
| pubmed-article:6789676 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:6789676 | pubmed:volume | 33 | lld:pubmed |
| pubmed-article:6789676 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:6789676 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:6789676 | pubmed:pagination | 640-8 | lld:pubmed |
| pubmed-article:6789676 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:meshHeading | pubmed-meshheading:6789676-... | lld:pubmed |
| pubmed-article:6789676 | pubmed:year | 1981 | lld:pubmed |
| pubmed-article:6789676 | pubmed:articleTitle | Detection of genetic variation with radioactive ligands. IV. X-linked, polymorphic genetic variation of thyroxin-binding globulin (TBG). | lld:pubmed |
| pubmed-article:6789676 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:6789676 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:6789676 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:6789676 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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