| pubmed-article:10877983 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10877983 | lifeskim:mentions | umls-concept:C0332307 | lld:lifeskim |
| pubmed-article:10877983 | lifeskim:mentions | umls-concept:C0039075 | lld:lifeskim |
| pubmed-article:10877983 | lifeskim:mentions | umls-concept:C0008633 | lld:lifeskim |
| pubmed-article:10877983 | lifeskim:mentions | umls-concept:C0079429 | lld:lifeskim |
| pubmed-article:10877983 | lifeskim:mentions | umls-concept:C0475264 | lld:lifeskim |
| pubmed-article:10877983 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:10877983 | pubmed:dateCreated | 2000-8-21 | lld:pubmed |
| pubmed-article:10877983 | pubmed:abstractText | Syndactyly type 1 (SD1) is an autosomal dominant limb malformation characterized in its classical form by complete or partial webbing between the third and fourth fingers and/or the second and third toes. After exclusion of a candidate region previously identified for syndactyly type 2 (synpolydactyly), we performed a genomewide linkage analysis in a large German pedigree. We found evidence for linkage of SD1 to polymorphic markers on chromosome 2q34-q36, with a maximum LOD score of 12.40 for marker D2S301. Key recombination events in affected individuals defined a 9.4-cM region between markers D2S2319 and D2S344. The identification of the responsible gene will give further insights into the molecular basis of limb development. | lld:pubmed |
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| pubmed-article:10877983 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10877983 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10877983 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:10877983 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10877983 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:10877983 | pubmed:issn | 0002-9297 | lld:pubmed |
| pubmed-article:10877983 | pubmed:author | pubmed-author:ReidRR | lld:pubmed |
| pubmed-article:10877983 | pubmed:author | pubmed-author:ProppingPP | lld:pubmed |
| pubmed-article:10877983 | pubmed:author | pubmed-author:WienkerT FTF | lld:pubmed |
| pubmed-article:10877983 | pubmed:author | pubmed-author:BossaGG | lld:pubmed |
| pubmed-article:10877983 | pubmed:author | pubmed-author:ZhuM DMD | lld:pubmed |
| pubmed-article:10877983 | pubmed:author | pubmed-author:NöthenM MMM | lld:pubmed |
| pubmed-article:10877983 | pubmed:author | pubmed-author:CichonSS | lld:pubmed |
| pubmed-article:10877983 | pubmed:author | pubmed-author:BetzR CRC | lld:pubmed |
| pubmed-article:10877983 | pubmed:author | pubmed-author:KleenHH | lld:pubmed |
| pubmed-article:10877983 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10877983 | pubmed:volume | 67 | lld:pubmed |
| pubmed-article:10877983 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10877983 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10877983 | pubmed:pagination | 492-7 | lld:pubmed |
| pubmed-article:10877983 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:10877983 | pubmed:meshHeading | pubmed-meshheading:10877983... | lld:pubmed |
| pubmed-article:10877983 | pubmed:meshHeading | pubmed-meshheading:10877983... | lld:pubmed |
| pubmed-article:10877983 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:10877983 | pubmed:articleTitle | Localization of a gene for syndactyly type 1 to chromosome 2q34-q36. | lld:pubmed |
| pubmed-article:10877983 | pubmed:affiliation | Institute of Human Genetics, University of Bonn, Germany. | lld:pubmed |
| pubmed-article:10877983 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10877983 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:57306 | entrezgene:pubmed | pubmed-article:10877983 | lld:entrezgene |
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