| pubmed-article:9429143 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9429143 | lifeskim:mentions | umls-concept:C0265215 | lld:lifeskim |
| pubmed-article:9429143 | lifeskim:mentions | umls-concept:C0242960 | lld:lifeskim |
| pubmed-article:9429143 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:9429143 | pubmed:dateCreated | 1998-2-4 | lld:pubmed |
| pubmed-article:9429143 | pubmed:abstractText | Meckel syndrome (MKS) is a lethal, autosomal recessive condition characterised by an occipital meningoencephalocele, enlarged kidneys with multicystic dysplasia, fibrotic changes of the liver in the portal area with ductal proliferation, and postaxial polydactyly. Recently, a MKS gene has been mapped to chromosome 17q21-q24 in Finnish families, with no evidence of locus heterogeneity in this population. Here, we report the exclusion of chromosome 17q21-q24 in eight typical MKS families of North African and Middle Eastern ancestry and provide evidence for genetic heterogeneity of this condition. | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9429143 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9429143 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9429143 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9429143 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:9429143 | pubmed:issn | 0022-2593 | lld:pubmed |
| pubmed-article:9429143 | pubmed:author | pubmed-author:MunnichAA | lld:pubmed |
| pubmed-article:9429143 | pubmed:author | pubmed-author:RoumeJJ | lld:pubmed |
| pubmed-article:9429143 | pubmed:author | pubmed-author:Le MerrerMM | lld:pubmed |
| pubmed-article:9429143 | pubmed:author | pubmed-author:MaH WHW | lld:pubmed |
| pubmed-article:9429143 | pubmed:author | pubmed-author:Cormier-Daire... | lld:pubmed |
| pubmed-article:9429143 | pubmed:author | pubmed-author:GirlichDD | lld:pubmed |
| pubmed-article:9429143 | pubmed:author | pubmed-author:GeninEE | lld:pubmed |
| pubmed-article:9429143 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9429143 | pubmed:volume | 34 | lld:pubmed |
| pubmed-article:9429143 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9429143 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9429143 | pubmed:pagination | 1003-6 | lld:pubmed |
| pubmed-article:9429143 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:9429143 | pubmed:meshHeading | pubmed-meshheading:9429143-... | lld:pubmed |
| pubmed-article:9429143 | pubmed:meshHeading | pubmed-meshheading:9429143-... | lld:pubmed |
| pubmed-article:9429143 | pubmed:meshHeading | pubmed-meshheading:9429143-... | lld:pubmed |
| pubmed-article:9429143 | pubmed:meshHeading | pubmed-meshheading:9429143-... | lld:pubmed |
| pubmed-article:9429143 | pubmed:meshHeading | pubmed-meshheading:9429143-... | lld:pubmed |
| pubmed-article:9429143 | pubmed:meshHeading | pubmed-meshheading:9429143-... | lld:pubmed |
| pubmed-article:9429143 | pubmed:meshHeading | pubmed-meshheading:9429143-... | lld:pubmed |
| pubmed-article:9429143 | pubmed:meshHeading | pubmed-meshheading:9429143-... | lld:pubmed |
| pubmed-article:9429143 | pubmed:meshHeading | pubmed-meshheading:9429143-... | lld:pubmed |
| pubmed-article:9429143 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9429143 | pubmed:articleTitle | Genetic heterogeneity of Meckel syndrome. | lld:pubmed |
| pubmed-article:9429143 | pubmed:affiliation | Unité de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U-393, Hôpital des Enfants-Malades, Paris, France. | lld:pubmed |
| pubmed-article:9429143 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9429143 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9429143 | lld:pubmed |
