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| pubmed-article:15689449 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
| pubmed-article:15689449 | lifeskim:mentions | umls-concept:C0243070 | lld:lifeskim |
| pubmed-article:15689449 | lifeskim:mentions | umls-concept:C0439064 | lld:lifeskim |
| pubmed-article:15689449 | lifeskim:mentions | umls-concept:C1510941 | lld:lifeskim |
| pubmed-article:15689449 | lifeskim:mentions | umls-concept:C1705938 | lld:lifeskim |
| pubmed-article:15689449 | lifeskim:mentions | umls-concept:C1527178 | lld:lifeskim |
| pubmed-article:15689449 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:15689449 | pubmed:dateCreated | 2005-2-3 | lld:pubmed |
| pubmed-article:15689449 | pubmed:abstractText | Malformations are a major cause of morbidity and mortality in full term infants and genomic imbalances are a significant component of their aetiology. However, the causes of defects in many patients with multiple congenital malformations remain unexplained despite thorough clinical examination and laboratory investigations. | lld:pubmed |
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| pubmed-article:15689449 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15689449 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15689449 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15689449 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15689449 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:15689449 | pubmed:issn | 1468-6244 | lld:pubmed |
| pubmed-article:15689449 | pubmed:author | pubmed-author:DavidAA | lld:pubmed |
| pubmed-article:15689449 | pubmed:author | pubmed-author:RivalJ MJM | lld:pubmed |
| pubmed-article:15689449 | pubmed:author | pubmed-author:JoubertMM | lld:pubmed |
| pubmed-article:15689449 | pubmed:author | pubmed-author:FrebourgTT | lld:pubmed |
| pubmed-article:15689449 | pubmed:author | pubmed-author:Saugier-Veber... | lld:pubmed |
| pubmed-article:15689449 | pubmed:author | pubmed-author:JacquemontSS | lld:pubmed |
| pubmed-article:15689449 | pubmed:author | pubmed-author:Le CaignecCC | lld:pubmed |
| pubmed-article:15689449 | pubmed:author | pubmed-author:BocenoMM | lld:pubmed |
| pubmed-article:15689449 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:15689449 | pubmed:volume | 42 | lld:pubmed |
| pubmed-article:15689449 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15689449 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15689449 | pubmed:pagination | 121-8 | lld:pubmed |
| pubmed-article:15689449 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:15689449 | pubmed:meshHeading | pubmed-meshheading:15689449... | lld:pubmed |
| pubmed-article:15689449 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15689449 | pubmed:articleTitle | Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations. | lld:pubmed |
| pubmed-article:15689449 | pubmed:affiliation | Service de Génétique Médicale, Institut de Biologie, Centre Hospitalier Universitaire, 9, quai Moncousu, 44093 Nantes Cedex, France. lecaignec@hotmail.com | lld:pubmed |
| pubmed-article:15689449 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15689449 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:15689449 | pubmed:publicationType | Evaluation Studies | lld:pubmed |
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