| pubmed-article:9327261 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9327261 | lifeskim:mentions | umls-concept:C0036857 | lld:lifeskim |
| pubmed-article:9327261 | lifeskim:mentions | umls-concept:C0024554 | lld:lifeskim |
| pubmed-article:9327261 | lifeskim:mentions | umls-concept:C1553356 | lld:lifeskim |
| pubmed-article:9327261 | lifeskim:mentions | umls-concept:C0348026 | lld:lifeskim |
| pubmed-article:9327261 | lifeskim:mentions | umls-concept:C1839796 | lld:lifeskim |
| pubmed-article:9327261 | lifeskim:mentions | umls-concept:C0805586 | lld:lifeskim |
| pubmed-article:9327261 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:9327261 | pubmed:dateCreated | 1998-1-8 | lld:pubmed |
| pubmed-article:9327261 | pubmed:abstractText | A severely mentally retarded 20-year-old male adult with a marfanoid habitus reported since birth and dysmorphic features is described. A younger brother presented the same appearance at birth but died at 2 months of age following a cardiopathy. Despite some clinical differences, his features are very close to the Lujan-Fryns syndrome and to two unrelated girls described by de Die-Smulders et al. (1). This case shows the challenge that clinicians could have while investigating patients with mental retardation and marfanoid habitus for diagnosis and genetic counseling. | lld:pubmed |
| pubmed-article:9327261 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9327261 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9327261 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9327261 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9327261 | pubmed:issn | 1015-8146 | lld:pubmed |
| pubmed-article:9327261 | pubmed:author | pubmed-author:MégarbanéAA | lld:pubmed |
| pubmed-article:9327261 | pubmed:author | pubmed-author:ChammasCC | lld:pubmed |
| pubmed-article:9327261 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9327261 | pubmed:volume | 8 | lld:pubmed |
| pubmed-article:9327261 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9327261 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9327261 | pubmed:pagination | 195-200 | lld:pubmed |
| pubmed-article:9327261 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
| pubmed-article:9327261 | pubmed:meshHeading | pubmed-meshheading:9327261-... | lld:pubmed |
| pubmed-article:9327261 | pubmed:meshHeading | pubmed-meshheading:9327261-... | lld:pubmed |
| pubmed-article:9327261 | pubmed:meshHeading | pubmed-meshheading:9327261-... | lld:pubmed |
| pubmed-article:9327261 | pubmed:meshHeading | pubmed-meshheading:9327261-... | lld:pubmed |
| pubmed-article:9327261 | pubmed:meshHeading | pubmed-meshheading:9327261-... | lld:pubmed |
| pubmed-article:9327261 | pubmed:meshHeading | pubmed-meshheading:9327261-... | lld:pubmed |
| pubmed-article:9327261 | pubmed:meshHeading | pubmed-meshheading:9327261-... | lld:pubmed |
| pubmed-article:9327261 | pubmed:meshHeading | pubmed-meshheading:9327261-... | lld:pubmed |
| pubmed-article:9327261 | pubmed:meshHeading | pubmed-meshheading:9327261-... | lld:pubmed |
| pubmed-article:9327261 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9327261 | pubmed:articleTitle | Severe mental retardation with marfanoid habitus in a young Lebanese male. A diagnostic challenge. | lld:pubmed |
| pubmed-article:9327261 | pubmed:affiliation | Unité de Génétique Médicale, Faculté de Médecine, Université Saint-Joseph, Beyrouth, Liban. | lld:pubmed |
| pubmed-article:9327261 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9327261 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:9327261 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
