pubmed-article:16014698 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16014698 | lifeskim:mentions | umls-concept:C1333666 | lld:lifeskim |
pubmed-article:16014698 | lifeskim:mentions | umls-concept:C0205145 | lld:lifeskim |
pubmed-article:16014698 | lifeskim:mentions | umls-concept:C0015127 | lld:lifeskim |
pubmed-article:16014698 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:16014698 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
pubmed-article:16014698 | lifeskim:mentions | umls-concept:C1832702 | lld:lifeskim |
pubmed-article:16014698 | lifeskim:mentions | umls-concept:C0684162 | lld:lifeskim |
pubmed-article:16014698 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:16014698 | pubmed:dateCreated | 2006-3-9 | lld:pubmed |
pubmed-article:16014698 | pubmed:abstractText | Brachydactyly type A2 (OMIM 112600) is characterised by hypoplasia/aplasia of the second middle phalanx of the index finger and sometimes the little finger. BDA2 was first described by Mohr and Wriedt in a large Danish/Norwegian kindred and mutations in BMPR1B were recently demonstrated in two affected families. | lld:pubmed |
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pubmed-article:16014698 | pubmed:language | eng | lld:pubmed |
pubmed-article:16014698 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16014698 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:16014698 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16014698 | pubmed:month | Mar | lld:pubmed |
pubmed-article:16014698 | pubmed:issn | 1468-6244 | lld:pubmed |
pubmed-article:16014698 | pubmed:author | pubmed-author:EibergHH | lld:pubmed |
pubmed-article:16014698 | pubmed:author | pubmed-author:RosendahlKK | lld:pubmed |
pubmed-article:16014698 | pubmed:author | pubmed-author:HansenLL | lld:pubmed |
pubmed-article:16014698 | pubmed:author | pubmed-author:TommerupNN | lld:pubmed |
pubmed-article:16014698 | pubmed:author | pubmed-author:MundlosSS | lld:pubmed |
pubmed-article:16014698 | pubmed:author | pubmed-author:van der... | lld:pubmed |
pubmed-article:16014698 | pubmed:author | pubmed-author:KjaerK WKW | lld:pubmed |
pubmed-article:16014698 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:16014698 | pubmed:volume | 43 | lld:pubmed |
pubmed-article:16014698 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16014698 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16014698 | pubmed:pagination | 225-31 | lld:pubmed |
pubmed-article:16014698 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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pubmed-article:16014698 | pubmed:meshHeading | pubmed-meshheading:16014698... | lld:pubmed |
pubmed-article:16014698 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:16014698 | pubmed:articleTitle | A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2. | lld:pubmed |
pubmed-article:16014698 | pubmed:affiliation | Wilhelm Johannsen Centre for Functional Genome Research, Department of Medical Biochemistry and Genetics, University of Copenhagen, Denmark. klaus@medgen.ku.dk | lld:pubmed |
pubmed-article:16014698 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16014698 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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