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pubmed-article:11161813pubmed:abstractTextWe have developed an integrated map for a 35-cM area of human chromosome 8 surrounding the Langer-Giedion syndrome deletion region. This map spans from approximately 8q22 to 8q24 and includes 10 hybrid cell intervals, 89 polymorphic STSs, 118 ESTs, and 37 known genes or inferred gene homologies. The map locations of 25 genes including osteoprotegerin, syndecan-2, and autotaxin have been refined from the general locations previously reported. In addition, the map has been used to indicate the location of nine deletions in patients with Langer-Giedion syndrome and trichorhinophalangeal syndrome type I to demonstrate the potential usefulness of the map in the analysis of these complex syndromes. The map will also be of interest to anyone trying to clone positionally disease genes in this region, such as Cohen syndrome (8q22-q23), Klip-Feil syndrome (8q22.2), hereditary spastic paraplegia (8q24), and benign adult familial myoclonic epilepsy (8q23.3-q24.1).lld:pubmed
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pubmed-article:11161813pubmed:authorpubmed-author:HiltonM JMJlld:pubmed
pubmed-article:11161813pubmed:copyrightInfoCopyright 2001 Academic Press.lld:pubmed
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pubmed-article:11161813pubmed:pagination192-9lld:pubmed
pubmed-article:11161813pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:11161813pubmed:articleTitleAn integrated physical map of 8q22-q24: use in positional cloning and deletion analysis of Langer-Giedion syndrome.lld:pubmed
pubmed-article:11161813pubmed:affiliationDepartment of Biology and Biochemistry, University of Houston, Houston, Texas 77204, USA.lld:pubmed
pubmed-article:11161813pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11161813pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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