| pubmed-article:10780921 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10780921 | lifeskim:mentions | umls-concept:C0019904 | lld:lifeskim |
| pubmed-article:10780921 | lifeskim:mentions | umls-concept:C0265559 | lld:lifeskim |
| pubmed-article:10780921 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:10780921 | lifeskim:mentions | umls-concept:C0008630 | lld:lifeskim |
| pubmed-article:10780921 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:10780921 | lifeskim:mentions | umls-concept:C0449445 | lld:lifeskim |
| pubmed-article:10780921 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:10780921 | pubmed:dateCreated | 2001-1-26 | lld:pubmed |
| pubmed-article:10780921 | pubmed:abstractText | Acheiropodia is an autosomal recessive disease that results in hemimelia (lack of formation of the distal extremities). We performed a complete genome screen of seven members of an extended pedigree that included three siblings with acheiropodia. Homozygosity mapping was used to identify regions most likely to harbor the gene for acheiropodia in this pedigree. In these two key regions (14p and 7q), further genotyping of one additional affected member of this pedigree plus seven additional unaffected siblings provided evidence, through linkage analysis, that the 7q36 region contains the acheiropodia gene. In this region, a maximum two-point LOD score of 3.81 (4.2 with multipoint analysis) was achieved, and a homozygous haplotype spanning a region of 11.7 cM was seen in all affected in this pedigree. Finally, genotypic analysis of two additional cases of acheiropodia with no known relation to the other samples revealed homozygous sharing of a portion of the same haplotype on 7q36, which reduces the chromosomal location of the acheiropodia gene to an 8.6-cM region. Localization of this gene, at the screening level, by use of data from only three affected subjects, provides an example of how certain genes may be mapped by use of a minimal number of affected cases. | lld:pubmed |
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| pubmed-article:10780921 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10780921 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10780921 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:10780921 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10780921 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:10780921 | pubmed:issn | 0002-9297 | lld:pubmed |
| pubmed-article:10780921 | pubmed:author | pubmed-author:RocheEE | lld:pubmed |
| pubmed-article:10780921 | pubmed:author | pubmed-author:HauserJJ | lld:pubmed |
| pubmed-article:10780921 | pubmed:author | pubmed-author:PittmanSS | lld:pubmed |
| pubmed-article:10780921 | pubmed:author | pubmed-author:LeeD TDT | lld:pubmed |
| pubmed-article:10780921 | pubmed:author | pubmed-author:FreimerN BNB | lld:pubmed |
| pubmed-article:10780921 | pubmed:author | pubmed-author:BenavidesEE | lld:pubmed |
| pubmed-article:10780921 | pubmed:author | pubmed-author:AlmasyLL | lld:pubmed |
| pubmed-article:10780921 | pubmed:author | pubmed-author:WhittleM RMR | lld:pubmed |
| pubmed-article:10780921 | pubmed:author | pubmed-author:EscamillaM... | lld:pubmed |
| pubmed-article:10780921 | pubmed:author | pubmed-author:DeMilleM CMC | lld:pubmed |
| pubmed-article:10780921 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10780921 | pubmed:volume | 66 | lld:pubmed |
| pubmed-article:10780921 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10780921 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10780921 | pubmed:pagination | 1995-2000 | lld:pubmed |
| pubmed-article:10780921 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:10780921 | pubmed:meshHeading | pubmed-meshheading:10780921... | lld:pubmed |
| pubmed-article:10780921 | pubmed:meshHeading | pubmed-meshheading:10780921... | lld:pubmed |
| pubmed-article:10780921 | pubmed:meshHeading | pubmed-meshheading:10780921... | lld:pubmed |
| pubmed-article:10780921 | pubmed:meshHeading | pubmed-meshheading:10780921... | lld:pubmed |
| pubmed-article:10780921 | pubmed:meshHeading | pubmed-meshheading:10780921... | lld:pubmed |
| pubmed-article:10780921 | pubmed:meshHeading | pubmed-meshheading:10780921... | lld:pubmed |
| pubmed-article:10780921 | pubmed:meshHeading | pubmed-meshheading:10780921... | lld:pubmed |
| pubmed-article:10780921 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:10780921 | pubmed:articleTitle | A minimalist approach to gene mapping: locating the gene for acheiropodia, by homozygosity analysis. | lld:pubmed |
| pubmed-article:10780921 | pubmed:affiliation | Neurogenetics Laboratory, Department of Psychiatry, University of Texas Health Science Center, San Antonio, TX, USA. escamillam@uthscsa.edu | lld:pubmed |
| pubmed-article:10780921 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10780921 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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