| pubmed-article:18156436 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18156436 | lifeskim:mentions | umls-concept:C0043210 | lld:lifeskim |
| pubmed-article:18156436 | lifeskim:mentions | umls-concept:C0040300 | lld:lifeskim |
| pubmed-article:18156436 | lifeskim:mentions | umls-concept:C0043297 | lld:lifeskim |
| pubmed-article:18156436 | lifeskim:mentions | umls-concept:C0439064 | lld:lifeskim |
| pubmed-article:18156436 | lifeskim:mentions | umls-concept:C1707455 | lld:lifeskim |
| pubmed-article:18156436 | lifeskim:mentions | umls-concept:C0449774 | lld:lifeskim |
| pubmed-article:18156436 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:18156436 | pubmed:dateCreated | 2008-4-29 | lld:pubmed |
| pubmed-article:18156436 | pubmed:abstractText | X-chromosome inactivation (XCI) is the mechanism by which gene dosage uniformity is achieved between female mammals with two X chromosomes and male mammals with a single X chromosome, and is thought to occur randomly. For molecular genetic testing, accessible tissues (eg blood) are commonly studied, but the relationship with inaccessible tissues (eg brain) is poorly understood. For accessible tissues to be informative for genetic analysis, a high degree of concordance of genetic findings among tissue types is required. | lld:pubmed |
| pubmed-article:18156436 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18156436 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18156436 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18156436 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18156436 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:18156436 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18156436 | pubmed:month | May | lld:pubmed |
| pubmed-article:18156436 | pubmed:issn | 1468-6244 | lld:pubmed |
| pubmed-article:18156436 | pubmed:author | pubmed-author:FischerWW | lld:pubmed |
| pubmed-article:18156436 | pubmed:author | pubmed-author:ButlerM GMG | lld:pubmed |
| pubmed-article:18156436 | pubmed:author | pubmed-author:BittelD CDC | lld:pubmed |
| pubmed-article:18156436 | pubmed:author | pubmed-author:TalebizadehZZ | lld:pubmed |
| pubmed-article:18156436 | pubmed:author | pubmed-author:KibiryevaNN | lld:pubmed |
| pubmed-article:18156436 | pubmed:author | pubmed-author:TheodoroM FMF | lld:pubmed |
| pubmed-article:18156436 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18156436 | pubmed:volume | 45 | lld:pubmed |
| pubmed-article:18156436 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18156436 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18156436 | pubmed:pagination | 309-13 | lld:pubmed |
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| pubmed-article:18156436 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18156436 | pubmed:articleTitle | Comparison of X-chromosome inactivation patterns in multiple tissues from human females. | lld:pubmed |
| pubmed-article:18156436 | pubmed:affiliation | Section of Medical Genetics and Molecular Medicine, Children's Mercy Hospitals and Clinics and University of Missouri - Kansas City School of Medicine, Kansas City, Missouri 64108, USA. | lld:pubmed |
| pubmed-article:18156436 | pubmed:publicationType | Letter | lld:pubmed |
| pubmed-article:18156436 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:18156436 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:18156436 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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