| pubmed-article:2222922 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2222922 | lifeskim:mentions | umls-concept:C0025266 | lld:lifeskim |
| pubmed-article:2222922 | lifeskim:mentions | umls-concept:C0026351 | lld:lifeskim |
| pubmed-article:2222922 | lifeskim:mentions | umls-concept:C0004268 | lld:lifeskim |
| pubmed-article:2222922 | lifeskim:mentions | umls-concept:C1136249 | lld:lifeskim |
| pubmed-article:2222922 | lifeskim:mentions | umls-concept:C0348026 | lld:lifeskim |
| pubmed-article:2222922 | lifeskim:mentions | umls-concept:C0314603 | lld:lifeskim |
| pubmed-article:2222922 | lifeskim:mentions | umls-concept:C0683326 | lld:lifeskim |
| pubmed-article:2222922 | lifeskim:mentions | umls-concept:C0038951 | lld:lifeskim |
| pubmed-article:2222922 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:2222922 | pubmed:dateCreated | 1990-12-20 | lld:pubmed |
| pubmed-article:2222922 | pubmed:abstractText | In this paper we report the results of a genetic-diagnostic survey of 274 institutionalized moderately mentally retarded adult males and compare these data with those from our previous studies in the severely mentally retarded and from a comparable population of 262 institutionalized moderately mentally retarded males and females (The Borgenstein experience). Special attention is paid to the nosology of X-linked mental retardation and familial mental retardation in general. | lld:pubmed |
| pubmed-article:2222922 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2222922 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2222922 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:2222922 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2222922 | pubmed:issn | 1015-8146 | lld:pubmed |
| pubmed-article:2222922 | pubmed:author | pubmed-author:van den... | lld:pubmed |
| pubmed-article:2222922 | pubmed:author | pubmed-author:FrynsJ PJP | lld:pubmed |
| pubmed-article:2222922 | pubmed:author | pubmed-author:DereymaekerA... | lld:pubmed |
| pubmed-article:2222922 | pubmed:author | pubmed-author:VolckePP | lld:pubmed |
| pubmed-article:2222922 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2222922 | pubmed:volume | 1 | lld:pubmed |
| pubmed-article:2222922 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2222922 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2222922 | pubmed:pagination | 47-56 | lld:pubmed |
| pubmed-article:2222922 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:meshHeading | pubmed-meshheading:2222922-... | lld:pubmed |
| pubmed-article:2222922 | pubmed:year | 1990 | lld:pubmed |
| pubmed-article:2222922 | pubmed:articleTitle | On the nosology of moderate mental retardation with special attention to X-linked mental retardation. A diagnostic genetic survey of 274 institutionalized moderately mentally retarded men. | lld:pubmed |
| pubmed-article:2222922 | pubmed:affiliation | Center for Human Genetics, University of Leuven, Belgium. | lld:pubmed |
| pubmed-article:2222922 | pubmed:publicationType | Journal Article | lld:pubmed |
