| pubmed-article:2988331 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2988331 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:2988331 | lifeskim:mentions | umls-concept:C0013264 | lld:lifeskim |
| pubmed-article:2988331 | lifeskim:mentions | umls-concept:C0205147 | lld:lifeskim |
| pubmed-article:2988331 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:2988331 | lifeskim:mentions | umls-concept:C1442161 | lld:lifeskim |
| pubmed-article:2988331 | lifeskim:mentions | umls-concept:C0162326 | lld:lifeskim |
| pubmed-article:2988331 | lifeskim:mentions | umls-concept:C1283195 | lld:lifeskim |
| pubmed-article:2988331 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:2988331 | pubmed:dateCreated | 1985-7-15 | lld:pubmed |
| pubmed-article:2988331 | pubmed:abstractText | A somatic cell hybrid has been constructed and characterized using fibroblasts from a phenotypically normal woman who possesses an X chromosome with an interstitial deletion of the short arm. High-resolution banding indicates that the deleted segment is either Xp22.13-p11.4 or Xp22.11-p11.23. Southern blot hybridization to previously mapped DNA sequences confirms that the missing segment of the X chromosome is a deletion and not an interstitial translocation and supports the cytogenetic interpretation that the deletion extends proximal of Xp11.3 and therefore probably comprises Xp22.11-p11.23. Three further DNA sequences have been localized to the region of the deleted segment. The following order has been assigned to the seven probes used: Xpter-RC8-pXUT22-(OA1,C7,M2C)-L1.28-RD6 -Xcen. | lld:pubmed |
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| pubmed-article:2988331 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2988331 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2988331 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:2988331 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2988331 | pubmed:month | May | lld:pubmed |
| pubmed-article:2988331 | pubmed:issn | 0002-9297 | lld:pubmed |
| pubmed-article:2988331 | pubmed:author | pubmed-author:WillardH FHF | lld:pubmed |
| pubmed-article:2988331 | pubmed:author | pubmed-author:WilliamsonRR | lld:pubmed |
| pubmed-article:2988331 | pubmed:author | pubmed-author:de la... | lld:pubmed |
| pubmed-article:2988331 | pubmed:author | pubmed-author:BatesGG | lld:pubmed |
| pubmed-article:2988331 | pubmed:author | pubmed-author:DaviesK EKE | lld:pubmed |
| pubmed-article:2988331 | pubmed:author | pubmed-author:PearsonPP | lld:pubmed |
| pubmed-article:2988331 | pubmed:author | pubmed-author:HaapalaKK | lld:pubmed |
| pubmed-article:2988331 | pubmed:author | pubmed-author:IngleCC | lld:pubmed |
| pubmed-article:2988331 | pubmed:author | pubmed-author:HervaR RRR | lld:pubmed |
| pubmed-article:2988331 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2988331 | pubmed:volume | 37 | lld:pubmed |
| pubmed-article:2988331 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2988331 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2988331 | pubmed:pagination | 451-62 | lld:pubmed |
| pubmed-article:2988331 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:2988331 | pubmed:year | 1985 | lld:pubmed |
| pubmed-article:2988331 | pubmed:articleTitle | Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation. | lld:pubmed |
| pubmed-article:2988331 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2988331 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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