| pubmed-article:1952789 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1952789 | lifeskim:mentions | umls-concept:C0022283 | lld:lifeskim |
| pubmed-article:1952789 | lifeskim:mentions | umls-concept:C0008625 | lld:lifeskim |
| pubmed-article:1952789 | lifeskim:mentions | umls-concept:C0039082 | lld:lifeskim |
| pubmed-article:1952789 | lifeskim:mentions | umls-concept:C1314939 | lld:lifeskim |
| pubmed-article:1952789 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:1952789 | pubmed:dateCreated | 1991-12-4 | lld:pubmed |
| pubmed-article:1952789 | pubmed:abstractText | The authors report on cytogenetic results of six patients with hypomelanosis of Ito. Karyotypes from peripheral lymphocytes prometaphases and skin fibroblasts metaphases were normal. A review of the literature revealed no specific chromosomal abnormality but a close association between mosaicism and HI syndrome. The X-chromosome was involved in 53% of the abnormal cases. | lld:pubmed |
| pubmed-article:1952789 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1952789 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1952789 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:1952789 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1952789 | pubmed:issn | 0003-3995 | lld:pubmed |
| pubmed-article:1952789 | pubmed:author | pubmed-author:BattistellaP... | lld:pubmed |
| pubmed-article:1952789 | pubmed:author | pubmed-author:PesericoAA | lld:pubmed |
| pubmed-article:1952789 | pubmed:author | pubmed-author:BaccichettiCC | lld:pubmed |
| pubmed-article:1952789 | pubmed:author | pubmed-author:LenziniEE | lld:pubmed |
| pubmed-article:1952789 | pubmed:author | pubmed-author:ArtifoniLL | lld:pubmed |
| pubmed-article:1952789 | pubmed:author | pubmed-author:BertoliPP | lld:pubmed |
| pubmed-article:1952789 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1952789 | pubmed:volume | 34 | lld:pubmed |
| pubmed-article:1952789 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1952789 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1952789 | pubmed:pagination | 30-2 | lld:pubmed |
| pubmed-article:1952789 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:meshHeading | pubmed-meshheading:1952789-... | lld:pubmed |
| pubmed-article:1952789 | pubmed:year | 1991 | lld:pubmed |
| pubmed-article:1952789 | pubmed:articleTitle | Hypomelanosis of Ito: involvement of chromosome aberrations in this syndrome. | lld:pubmed |
| pubmed-article:1952789 | pubmed:affiliation | Servizio di Genetica Medica, Dipartimento di Pediatria, Università di Padova, Italy. | lld:pubmed |
| pubmed-article:1952789 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1952789 | pubmed:publicationType | Review | lld:pubmed |
