| pubmed-article:20300295 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20300295 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:20300295 | lifeskim:mentions | umls-concept:C0019069 | lld:lifeskim |
| pubmed-article:20300295 | lifeskim:mentions | umls-concept:C0020792 | lld:lifeskim |
| pubmed-article:20300295 | lifeskim:mentions | umls-concept:C0020202 | lld:lifeskim |
| pubmed-article:20300295 | lifeskim:mentions | umls-concept:C1704822 | lld:lifeskim |
| pubmed-article:20300295 | lifeskim:mentions | umls-concept:C1366370 | lld:lifeskim |
| pubmed-article:20300295 | lifeskim:mentions | umls-concept:C0596611 | lld:lifeskim |
| pubmed-article:20300295 | lifeskim:mentions | umls-concept:C2732002 | lld:lifeskim |
| pubmed-article:20300295 | lifeskim:mentions | umls-concept:C1561491 | lld:lifeskim |
| pubmed-article:20300295 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:20300295 | pubmed:dateCreated | 2010-3-19 | lld:pubmed |
| pubmed-article:20300295 | pubmed:abstractText | Standard methods of mutation detection are time consuming in Hemophilia A (HA) rendering their application unavailable in some analysis such as prenatal diagnosis. | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20300295 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20300295 | pubmed:status | PubMed-not-MEDLINE | lld:pubmed |
| pubmed-article:20300295 | pubmed:month | May | lld:pubmed |
| pubmed-article:20300295 | pubmed:issn | 0971-6866 | lld:pubmed |
| pubmed-article:20300295 | pubmed:author | pubmed-author:SurreySS | lld:pubmed |
| pubmed-article:20300295 | pubmed:author | pubmed-author:FortinaPP | lld:pubmed |
| pubmed-article:20300295 | pubmed:author | pubmed-author:ChettyUU | lld:pubmed |
| pubmed-article:20300295 | pubmed:author | pubmed-author:MargaglioneMM | lld:pubmed |
| pubmed-article:20300295 | pubmed:author | pubmed-author:GrandoneEE | lld:pubmed |
| pubmed-article:20300295 | pubmed:author | pubmed-author:SantacroceRR | lld:pubmed |
| pubmed-article:20300295 | pubmed:author | pubmed-author:DrmanacAA | lld:pubmed |
| pubmed-article:20300295 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:20300295 | pubmed:volume | 14 | lld:pubmed |
| pubmed-article:20300295 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20300295 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20300295 | pubmed:pagination | 55-64 | lld:pubmed |
| pubmed-article:20300295 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:20300295 | pubmed:articleTitle | Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridization. | lld:pubmed |
| pubmed-article:20300295 | pubmed:publicationType | Journal Article | lld:pubmed |
