| pubmed-article:9859153 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9859153 | lifeskim:mentions | umls-concept:C0008972 | lld:lifeskim |
| pubmed-article:9859153 | lifeskim:mentions | umls-concept:C0027831 | lld:lifeskim |
| pubmed-article:9859153 | pubmed:issue | 159 | lld:pubmed |
| pubmed-article:9859153 | pubmed:dateCreated | 1999-2-17 | lld:pubmed |
| pubmed-article:9859153 | pubmed:abstractText | Recklinghausen's disease is considered to be the autosomal dominant disorder with the highest rate of mutation after achondroplasia. It is a neuroectodermal disorder with considerable clinical effects. | lld:pubmed |
| pubmed-article:9859153 | pubmed:language | spa | lld:pubmed |
| pubmed-article:9859153 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9859153 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9859153 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9859153 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:9859153 | pubmed:issn | 0210-0010 | lld:pubmed |
| pubmed-article:9859153 | pubmed:author | pubmed-author:ArgüellesMM | lld:pubmed |
| pubmed-article:9859153 | pubmed:author | pubmed-author:LozadaYY | lld:pubmed |
| pubmed-article:9859153 | pubmed:author | pubmed-author:Alvarez-Valie... | lld:pubmed |
| pubmed-article:9859153 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9859153 | pubmed:volume | 27 | lld:pubmed |
| pubmed-article:9859153 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9859153 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9859153 | pubmed:pagination | 792-5 | lld:pubmed |
| pubmed-article:9859153 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:meshHeading | pubmed-meshheading:9859153-... | lld:pubmed |
| pubmed-article:9859153 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9859153 | pubmed:articleTitle | [Clinical study of neurofibromatosis type 1]. | lld:pubmed |
| pubmed-article:9859153 | pubmed:affiliation | Departamento Provincial de Genética Clínica, Hospital Infantil Sur, Santiago de Cuba, Cuba. | lld:pubmed |
| pubmed-article:9859153 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9859153 | pubmed:publicationType | English Abstract | lld:pubmed |
