| pubmed-article:1376967 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1376967 | lifeskim:mentions | umls-concept:C0439660 | lld:lifeskim |
| pubmed-article:1376967 | lifeskim:mentions | umls-concept:C0149566 | lld:lifeskim |
| pubmed-article:1376967 | lifeskim:mentions | umls-concept:C0151636 | lld:lifeskim |
| pubmed-article:1376967 | lifeskim:mentions | umls-concept:C0751534 | lld:lifeskim |
| pubmed-article:1376967 | lifeskim:mentions | umls-concept:C0039082 | lld:lifeskim |
| pubmed-article:1376967 | lifeskim:mentions | umls-concept:C1519249 | lld:lifeskim |
| pubmed-article:1376967 | lifeskim:mentions | umls-concept:C0079411 | lld:lifeskim |
| pubmed-article:1376967 | lifeskim:mentions | umls-concept:C0000325 | lld:lifeskim |
| pubmed-article:1376967 | lifeskim:mentions | umls-concept:C0304016 | lld:lifeskim |
| pubmed-article:1376967 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:1376967 | pubmed:dateCreated | 1992-7-22 | lld:pubmed |
| pubmed-article:1376967 | pubmed:abstractText | We observed the combination of the Robin sequence with perodactyly (hypoplasia and/or agenesis of the distal phalanx of the toes) and cardiac arrhythmia (ventricular extrasystoles occurring as bigemini or multifocal tachycardia with syncopal episodes) in 6 relatives in 3 generations. This familial association has not been reported before and probably represents a previously unrecognized heritable malformation syndrome. | lld:pubmed |
| pubmed-article:1376967 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1376967 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1376967 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:1376967 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1376967 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:1376967 | pubmed:issn | 0148-7299 | lld:pubmed |
| pubmed-article:1376967 | pubmed:author | pubmed-author:StollCC | lld:pubmed |
| pubmed-article:1376967 | pubmed:author | pubmed-author:FinchPP | lld:pubmed |
| pubmed-article:1376967 | pubmed:author | pubmed-author:KienyJ RJR | lld:pubmed |
| pubmed-article:1376967 | pubmed:author | pubmed-author:DottBB | lld:pubmed |
| pubmed-article:1376967 | pubmed:author | pubmed-author:AlembikYY | lld:pubmed |
| pubmed-article:1376967 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1376967 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:1376967 | pubmed:volume | 42 | lld:pubmed |
| pubmed-article:1376967 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1376967 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1376967 | pubmed:pagination | 480-6 | lld:pubmed |
| pubmed-article:1376967 | pubmed:dateRevised | 2004-11-17 | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:meshHeading | pubmed-meshheading:1376967-... | lld:pubmed |
| pubmed-article:1376967 | pubmed:year | 1992 | lld:pubmed |
| pubmed-article:1376967 | pubmed:articleTitle | Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin in sequence in three generations: a new inherited MCA syndrome? | lld:pubmed |
| pubmed-article:1376967 | pubmed:affiliation | Institut de Puériculture, Centre Hospitalo-Universitaire, Strasbourg, France. | lld:pubmed |
| pubmed-article:1376967 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1376967 | pubmed:publicationType | Case Reports | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:1376967 | lld:pubmed |
