pubmed-article:3177466 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:3177466 | lifeskim:mentions | umls-concept:C1136249 | lld:lifeskim |
pubmed-article:3177466 | lifeskim:mentions | umls-concept:C0376315 | lld:lifeskim |
pubmed-article:3177466 | lifeskim:mentions | umls-concept:C1704666 | lld:lifeskim |
pubmed-article:3177466 | lifeskim:mentions | umls-concept:C1517892 | lld:lifeskim |
pubmed-article:3177466 | lifeskim:mentions | umls-concept:C0208973 | lld:lifeskim |
pubmed-article:3177466 | pubmed:issue | 1-2 | lld:pubmed |
pubmed-article:3177466 | pubmed:dateCreated | 1988-11-8 | lld:pubmed |
pubmed-article:3177466 | pubmed:abstractText | An analysis of the linkage of a non-syndromal form of X-linked mental retardation (MRX1) with a number of markers on the X chromosome was performed in a large pedigree. The affected males had moderate mental retardation; in all other clinical respects and cytogenetically they were normal. No recombinants were observed between the MRX1 gene and the marker DXS14 (p58.1) located at Xp11-cen (Z (max.) = 2.12 at theta = 0.00). Recombination was observed between the MRX1 gene and the markers DXS7 and DXYS1 which flank DXS14. This form of XLMR maps to the centromeric portion of the X-chromosome. | lld:pubmed |
pubmed-article:3177466 | pubmed:language | eng | lld:pubmed |
pubmed-article:3177466 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3177466 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:3177466 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3177466 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:3177466 | pubmed:issn | 0148-7299 | lld:pubmed |
pubmed-article:3177466 | pubmed:author | pubmed-author:TurnerGG | lld:pubmed |
pubmed-article:3177466 | pubmed:author | pubmed-author:MulleyJ CJC | lld:pubmed |
pubmed-article:3177466 | pubmed:author | pubmed-author:SuthersG KGK | lld:pubmed |
pubmed-article:3177466 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:3177466 | pubmed:volume | 30 | lld:pubmed |
pubmed-article:3177466 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:3177466 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:3177466 | pubmed:pagination | 485-91 | lld:pubmed |
pubmed-article:3177466 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
pubmed-article:3177466 | pubmed:meshHeading | pubmed-meshheading:3177466-... | lld:pubmed |
pubmed-article:3177466 | pubmed:meshHeading | pubmed-meshheading:3177466-... | lld:pubmed |
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pubmed-article:3177466 | pubmed:meshHeading | pubmed-meshheading:3177466-... | lld:pubmed |
pubmed-article:3177466 | pubmed:meshHeading | pubmed-meshheading:3177466-... | lld:pubmed |
pubmed-article:3177466 | pubmed:meshHeading | pubmed-meshheading:3177466-... | lld:pubmed |
pubmed-article:3177466 | pubmed:articleTitle | A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14. | lld:pubmed |
pubmed-article:3177466 | pubmed:affiliation | Department of Histopathology, Adelaide Children's Hospital, South Australia. | lld:pubmed |
pubmed-article:3177466 | pubmed:publicationType | Journal Article | lld:pubmed |
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