| pubmed-article:9835963 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9835963 | lifeskim:mentions | umls-concept:C0332307 | lld:lifeskim |
| pubmed-article:9835963 | lifeskim:mentions | umls-concept:C0037285 | lld:lifeskim |
| pubmed-article:9835963 | lifeskim:mentions | umls-concept:C0007004 | lld:lifeskim |
| pubmed-article:9835963 | lifeskim:mentions | umls-concept:C0017968 | lld:lifeskim |
| pubmed-article:9835963 | lifeskim:mentions | umls-concept:C0376322 | lld:lifeskim |
| pubmed-article:9835963 | lifeskim:mentions | umls-concept:C0039082 | lld:lifeskim |
| pubmed-article:9835963 | lifeskim:mentions | umls-concept:C0011155 | lld:lifeskim |
| pubmed-article:9835963 | lifeskim:mentions | umls-concept:C1280464 | lld:lifeskim |
| pubmed-article:9835963 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:9835963 | pubmed:dateCreated | 1998-12-21 | lld:pubmed |
| pubmed-article:9835963 | pubmed:abstractText | Type I carbohydrate deficient glycoprotein (CDG) syndrome is an inborn hereditary error of metabolism with a broad clinical spectrum. It is characterized by partial N-glycan deficiency of glycoproteins. Skin features may be part of this syndrome in infancy. | lld:pubmed |
| pubmed-article:9835963 | pubmed:language | fre | lld:pubmed |
| pubmed-article:9835963 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9835963 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9835963 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9835963 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9835963 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9835963 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9835963 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9835963 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:9835963 | pubmed:issn | 0151-9638 | lld:pubmed |
| pubmed-article:9835963 | pubmed:author | pubmed-author:de ProstYY | lld:pubmed |
| pubmed-article:9835963 | pubmed:author | pubmed-author:SaudubrayJ... | lld:pubmed |
| pubmed-article:9835963 | pubmed:author | pubmed-author:AmoricJ CJC | lld:pubmed |
| pubmed-article:9835963 | pubmed:author | pubmed-author:VabresPP | lld:pubmed |
| pubmed-article:9835963 | pubmed:author | pubmed-author:SevinCC | lld:pubmed |
| pubmed-article:9835963 | pubmed:author | pubmed-author:OdièvreM HMH | lld:pubmed |
| pubmed-article:9835963 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9835963 | pubmed:volume | 125 | lld:pubmed |
| pubmed-article:9835963 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9835963 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9835963 | pubmed:pagination | 715-6 | lld:pubmed |
| pubmed-article:9835963 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:meshHeading | pubmed-meshheading:9835963-... | lld:pubmed |
| pubmed-article:9835963 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9835963 | pubmed:articleTitle | [Skin manifestations of protein glycosylation deficiency, the CDG (carbohydrate deficient glycoprotein) type 1 syndrome]. | lld:pubmed |
| pubmed-article:9835963 | pubmed:affiliation | Service de Dermatologie, Hôpital Necker-Enfants Malades, Paris. | lld:pubmed |
| pubmed-article:9835963 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9835963 | pubmed:publicationType | English Abstract | lld:pubmed |
| pubmed-article:9835963 | pubmed:publicationType | Case Reports | lld:pubmed |
