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pubmed-article:1981049pubmed:abstractTextA refined genetic linkage map for the pericentromeric region of human chromosome 10 has been constructed from data on 12 distinct polymorphic DNA loci as well as the locus for multiple endocrine neoplasia type 2A (MEN 2A), a dominantly inherited cancer syndrome. The map extends from D10S24 (at 10p13-p12.2) to D10S3 (at 10q21-q23) and is about 70 cM long. Overall, higher female than male recombination frequencies were observed for this region, with the most remarkable female excess in the immediate vicinity of the centromere, as previously reported. Most of the DNA markers in this map are highly informative for linkage and the majority of the interlocus intervals are no more than 6 cM apart. Thus this map should provide a fine framework for future efforts in more detailed mapping studies around the centromeric area. A set of ordered cross-overs identified in this work is a valuable resource for rapidly and accurately localizing new DNA clones isolated from the pericentromeric region.lld:pubmed
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pubmed-article:1981049pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:1981049pubmed:articleTitleA refined linkage map for DNA markers around the pericentromeric region of chromosome 10.lld:pubmed
pubmed-article:1981049pubmed:affiliationDepartment of Human Genetics, Yale University School of Medicine, New Haven, Connecticut 06510.lld:pubmed
pubmed-article:1981049pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1981049pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:1981049pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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